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Incidence Statistics for Types of Nervous system conditions

The information below shows a list of types of Nervous system conditions, with information as to the annual incidence of each of these types of Nervous system conditions. Estimates of the people affected each year are calculated based on the available statistics.

Incidence Statistics for Types of Nervous system conditions

Disease

Incidence Estimate

US people estimate

Statistic Used for Calculation

Toxic polyneuropathy -- Agenerase N/A N/A No information
Toxic polyneuropathy -- Amiodarone N/A N/A No information
Toxic polyneuropathy -- Amitriptyline N/A N/A No information
Toxic polyneuropathy -- Amphotericin N/A N/A No information
Toxic polyneuropathy -- Amprenavir N/A N/A No information
Toxic polyneuropathy -- Arsenic N/A N/A No information
Toxic polyneuropathy -- Calcium Carbimide N/A N/A No information
Toxic polyneuropathy -- acrylamide N/A N/A No information
Toxic polyneuropathy -- Carbon disulfide N/A N/A No information
Toxic polyneuropathy -- Carbutamide N/A N/A No information
Toxic polyneuropathy -- Chlorambucil N/A N/A No information
Toxic polyneuropathy -- Chloramphenicol N/A N/A No information
Toxic polyneuropathy -- Chloroquine N/A N/A No information
Toxic polyneuropathy -- Chlorpropamide N/A N/A No information
Toxic polyneuropathy -- Cisplatin N/A N/A No information
Toxic polyneuropathy -- Clioquinol N/A N/A No information
Toxic polyneuropathy -- Clofibrate N/A N/A No information
Toxic polyneuropathy -- Colchicine N/A N/A No information
Toxic polyneuropathy -- Colistin N/A N/A No information
Toxic polyneuropathy -- Cytarabine N/A N/A No information
Toxic polyneuropathy -- Dapsone N/A N/A No information
Toxic polyneuropathy -- Diamines N/A N/A No information
Toxic polyneuropathy -- Didanosine N/A N/A No information
Toxic polyneuropathy -- Disopyramide N/A N/A No information
Toxic polyneuropathy -- Disulfiram N/A N/A No information
Toxic polyneuropathy -- Ergotamine N/A N/A No information
Toxic polyneuropathy -- Ethambutol N/A N/A No information
Toxic polyneuropathy -- Ethionamide N/A N/A No information
Toxic polyneuropathy -- Ethoglucid N/A N/A No information
Toxic polyneuropathy -- Ethylene oxide N/A N/A No information
Toxic polyneuropathy -- Gemfibrozil N/A N/A No information
Toxic polyneuropathy -- Glutethimide N/A N/A No information
Toxic polyneuropathy -- Gold N/A N/A No information
Toxic polyneuropathy -- Hydralazine N/A N/A No information
Toxic polyneuropathy -- Indapamid N/A N/A No information
Toxic polyneuropathy -- Indomethacin N/A N/A No information
Toxic polyneuropathy -- Isoniazid N/A N/A No information
Toxic polyneuropathy -- Lead N/A N/A No information
Toxic polyneuropathy -- Lopid N/A N/A No information
Toxic polyneuropathy -- Lovastatin N/A N/A No information
Toxic polyneuropathy -- Lozol N/A N/A No information
Toxic polyneuropathy -- Mercury N/A N/A No information
Toxic polyneuropathy -- Methaqualone N/A N/A No information
Toxic polyneuropathy -- Methimazole N/A N/A No information
Toxic polyneuropathy -- Methyl Bromide N/A N/A No information
Toxic polyneuropathy -- Methysergide N/A N/A No information
Toxic polyneuropathy -- Metronidazole N/A N/A No information
Toxic polyneuropathy -- Mevacor N/A N/A No information
Toxic polyneuropathy -- Mustine N/A N/A No information
Toxic polyneuropathy -- Nalidixic Acid N/A N/A No information
Toxic polyneuropathy -- Nitrofurantoin N/A N/A No information
Toxic polyneuropathy -- Nitrofurazone N/A N/A No information
Toxic polyneuropathy -- Norvir N/A N/A No information
Toxic polyneuropathy -- Perhexiline N/A N/A No information
Toxic polyneuropathy -- Phenelzine N/A N/A No information
Toxic polyneuropathy -- Phenylbutazone N/A N/A No information
Toxic polyneuropathy -- Phenytoin N/A N/A No information
Toxic polyneuropathy -- Podophyllum N/A N/A No information
Toxic polyneuropathy -- Polychlorinated biphenyls (PCBs) N/A N/A No information
Toxic polyneuropathy -- Procarbazine N/A N/A No information
Toxic polyneuropathy -- Propranolol N/A N/A No information
Toxic polyneuropathy -- Propylthiouracil N/A N/A No information
Toxic polyneuropathy -- Ritonavir N/A N/A No information
Toxic polyneuropathy -- Stavudine N/A N/A No information
Toxic polyneuropathy -- Streptomycin N/A N/A No information
Toxic polyneuropathy -- Sulfoxone N/A N/A No information
Toxic polyneuropathy -- Sulphonamide N/A N/A No information
Toxic polyneuropathy -- Sulthiame N/A N/A No information
Toxic polyneuropathy -- Thalidomide N/A N/A No information
Toxic polyneuropathy -- Thallium N/A N/A No information
Toxic polyneuropathy -- Thiamphenicol N/A N/A No information
Toxic polyneuropathy -- Tolbutamide N/A N/A No information
Toxic polyneuropathy -- Videx N/A N/A No information
Toxic polyneuropathy -- Vincristine N/A N/A No information
Toxic polyneuropathy -- Zalcitabine N/A N/A No information
Toxic polyneuropathy -- Zerit N/A N/A No information
Toxic polyneuropathy -- Zidovudine N/A N/A No information
Venezuelan Equine Encephalitis -- Teratogenic Agent N/A N/A No information
Syphilis -- Teratogenic Agent N/A N/A No information
Sound to Taste Synesthesia N/A N/A No information
Vision to Temperature Synesthesia N/A N/A No information
Vision to Touch Synesthesia N/A N/A No information
Vision to Taste Synesthesia N/A N/A No information
Vision to Sound Synesthesia N/A N/A No information
Vision to Smell Synesthesia N/A N/A No information
Touch to Temperature Synesthesia N/A N/A No information
Touch to Taste Synesthesia N/A N/A No information
Touch to Sound Synesthesia N/A N/A No information
Touch to Smell Synesthesia N/A N/A No information
Temperature to Sound Synesthesia N/A N/A No information
Taste to Touch Synesthesia N/A N/A No information
Taste to Temperature Synesthesia N/A N/A No information
Taste to Sound Synesthesia N/A N/A No information
Sound to Touch Synesthesia N/A N/A No information
Sound to Temperature Synesthesia N/A N/A No information
Sound to Smell Synesthesia N/A N/A No information
Sound to Kinetics Synesthesia N/A N/A No information
Smell to Touch Synesthesia N/A N/A No information
Smell to Temperature Synesthesia N/A N/A No information
Smell to Taste Synesthesia N/A N/A No information
Smell to Sound Synesthesia N/A N/A No information
Personality to Touch Synesthesia N/A N/A No information
Personality to Smell Synesthesia N/A N/A No information
Kinetics to Sound Synesthesia N/A N/A No information
Orgasm to Color Synesthesia N/A N/A No information
Temperature to Color Synesthesia N/A N/A No information
Touch to Color Synesthesia N/A N/A No information
Personalities to Color Synesthesia N/A N/A No information
Pain to Color Synesthesia N/A N/A No information
Odours to Color Synesthesia N/A N/A No information
Time Units to Color Synesthesia N/A N/A No information
Music to Color Synesthesia N/A N/A No information
Emotion to Color Synesthesia N/A N/A No information
Time to Space Synesthesia N/A N/A No information
Ordinal Personification N/A N/A No information
Shaped-Numbers N/A N/A No information
Colored-Graphemes N/A N/A No information
Colored-Letters N/A N/A No information
Colored-Numbers N/A N/A No information
Tactile-Gustation N/A N/A No information
Colored-Gustation N/A N/A No information
Colored-Olfaction N/A N/A No information
Colored Hearing N/A N/A No information
Two-Sensory Synesthesia N/A N/A No information
Multiple Sensory Synesthesia N/A N/A No information
Concussion-Induced Synesthesia N/A N/A No information
Spinal Cord Damage-Induced Synesthesia N/A N/A No information
Brain Damage-Induced Synesthesia N/A N/A No information
Neuron Degeneration-Induced Synesthesia N/A N/A No information
Drug-Induced Synesthesia N/A N/A No information
Epileptic synesthesia N/A N/A No information
Idiopathic Synesthesia N/A N/A No information
Acquired Synesthesia N/A N/A No information
Phantosmia N/A N/A No information
Metastatic nervous system cancer N/A N/A No information
Aneurysm, intracranial berry, 10 N/A N/A No information
Aneurysm, intracranial berry, 9 N/A N/A No information
Aneurysmal subarachnoid haemorrhage N/A N/A No information
Aneurysm, intracranial berry N/A N/A No information
Aneurysm, intracranial berry, 1 N/A N/A No information
Aneurysm, intracranial berry, 2 N/A N/A No information
Aneurysm, intracranial berry, 3 N/A N/A No information
Aneurysm, intracranial berry, 4 N/A N/A No information
Aneurysm, intracranial berry, 5 N/A N/A No information
Aneurysm, intracranial berry, 6 N/A N/A No information
Neurofibroma N/A N/A No information
Acoustic neuroma N/A N/A No information
Brain Stem Glioma N/A N/A No information
Medulloblastoma N/A N/A No information
Meningioma N/A N/A No information
Oligodendroglioma N/A N/A No information
Neuroblastoma N/A N/A No information
Meninges cancer N/A N/A No information
Brain cancer approx 1 in 16,000 or 0.01% or 17,000 people in USA 17,000 17,000 annual cases in USA (SEER 2002 estimate: brain and other nervous system)
Cerebrovascular Conditions N/A N/A No information
Stroke approx 1 in 453 or 0.22% or 600,000 people in USA 600,000 600,000 annually (CDC) including 500,000 new cases and 100,000 recurrences.
Cerebrovascular accident N/A N/A No information
Familial Febrile Convulsions, 2 N/A N/A No information
Spastic Paraplegia 42, Autosomal Dominant N/A N/A No information
Acute headache N/A N/A No information
Complicated migraine N/A N/A No information
Retinal migraine N/A N/A No information
Migrainous stupor migraine N/A N/A No information
Chronic paroxysmal hemicrania N/A N/A No information
Lower half headache N/A N/A No information
Benign exertional-sex headache N/A N/A No information
Exertional headache N/A N/A No information
Cervicogenic headache N/A N/A No information
Drug rebound headache N/A N/A No information
Gravitational headache N/A N/A No information
Icepick headache N/A N/A No information
Hypertension headache N/A N/A No information
Cough headache N/A N/A No information
Ice-cream headache N/A N/A No information
Facioplegic migraine N/A N/A No information
Headache N/A N/A No information
Common Headache approx 1 in 1 or 90.00% or 244.8 million people in USA 244,800,000 90% approximately; almost everyone gets some each year.
Migraine N/A N/A No information
Sexual headache N/A N/A No information
Cluster headache N/A N/A No information
Tension headache N/A N/A No information
Chronic headache N/A N/A No information
Vascular headaches N/A N/A No information
Exertional headaches N/A N/A No information
Post-traumatic headache N/A N/A No information
Classic migraine N/A N/A No information
Common migraine N/A N/A No information
Basilar artery migraine N/A N/A No information
Muscle contraction headache N/A N/A No information
Chronic tension headache N/A N/A No information
Temporal arteritis N/A N/A No information
Neuroblastoma, Susceptibility to, 6 N/A N/A No information
Neuroblastoma, Susceptibility to, 5 N/A N/A No information
Neuroblastoma, Susceptibility to, 4 N/A N/A No information
Neuroblastoma, Susceptibility to, 3 N/A N/A No information
Neuroblastoma, Susceptibility to, 2 N/A N/A No information
Neuroblastoma, Susceptibility to, 1 N/A N/A No information
Glioma Susceptibility 8 N/A N/A No information
Glioma Susceptibility 7 N/A N/A No information
Glioma Susceptibility 6 N/A N/A No information
Glioma Susceptibility 5 N/A N/A No information
Glioma Susceptibility 4 N/A N/A No information
Glioma Susceptibility 3 N/A N/A No information
Glioma Susceptibility 2 N/A N/A No information
Glioma Susceptibility 1 N/A N/A No information
Glioma Susceptibility N/A N/A No information
Lissencephaly 3 N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 6 N/A N/A No information
Spinocerebellar ataxia 18 N/A N/A No information
Spinocerebellar ataxia 27 N/A N/A No information
Spinocerebellar ataxia 19 N/A N/A No information
Spinocerebellar ataxia 28 N/A N/A No information
Spinocerebellar ataxia 29 N/A N/A No information
Spinocerebellar ataxia, autosomal dominant N/A N/A No information
Familial Febrile Convulsions, 3 N/A N/A No information
Familial Febrile Convulsions, 3A N/A N/A No information
Familial Febrile Convulsions, 3B N/A N/A No information
Familial Febrile Convulsions, 4 N/A N/A No information
Familial Febrile Convulsions, 5 N/A N/A No information
Familial Febrile Convulsions, 6 N/A N/A No information
Familial Febrile Convulsions, 7 N/A N/A No information
Familial Febrile Convulsions, 8 N/A N/A No information
Familial Febrile Convulsions, 9 N/A N/A No information
Familial Febrile Convulsions, 10 N/A N/A No information
Familial Febrile Convulsions, 1 N/A N/A No information
Familial Febrile Convulsions N/A N/A No information
Epilepsy, Benign Neonatal N/A N/A No information
Epilepsy, Benign Neonatal, 1 N/A N/A No information
Epilepsy, Benign Neonatal, 2 N/A N/A No information
Epilepsy, Benign Neonatal, 3 N/A N/A No information
Epilepsy, Benign Neonatal, Autosomal Recessive N/A N/A No information
Temporal epilepsy, familial N/A N/A No information
Generalized Epilepsy with Febrile Seizures Plus, type 2 N/A N/A No information
Generalized Epilepsy with Febrile Seizures Plus, type 3 N/A N/A No information
Generalized Epilepsy with Febrile Seizures Plus, type 5 N/A N/A No information
Generalized Epilepsy with Febrile Seizures Plus, type 4 N/A N/A No information
Generalized Epilepsy with Febrile Seizures Plus, type 6 N/A N/A No information
Generalized Epilepsy with Febrile Seizures Plus, type 1 N/A N/A No information
Generalized Epilepsy with Febrile Seizures Plus N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 21 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 30 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 12 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 31 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 13 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 22 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 15 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 24 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 41 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 23 N/A N/A No information
Tinnitus N/A N/A No information
Sensorineural deafness N/A N/A No information
Nerve deafness N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 4 N/A N/A No information
Spinocerebellar ataxia 16 N/A N/A No information
Spinocerebellar ataxia 25 N/A N/A No information
Dyslexia N/A N/A No information
Tourette Syndrome N/A N/A No information
Grand mal seizures N/A N/A No information
Petit mal seizures N/A N/A No information
Grand mal epilepsy N/A N/A No information
Petit mal epilepsy N/A N/A No information
Temporal lobe epilepsy N/A N/A No information
Status epilepticus N/A N/A No information
Spastic paraplegia 30, autosomal recessive N/A N/A No information
Intracranial germ cell tumour N/A N/A No information
Spastic paraplegia 32, autosomal recessive N/A N/A No information
Migraine with or without aura, susceptibility to, 10 N/A N/A No information
Migraine with or without aura, susceptibility to, 11 N/A N/A No information
Migraine with aura, susceptibility to, 9 N/A N/A No information
Spastic paraplegia 33, autosomal dominant N/A N/A No information
Neuropathy sensory spastic paraplegia N/A N/A No information
Spastic paraplegia 3, autosomal dominant N/A N/A No information
Charcot-Marie-Tooth disease, X-linked recessive, 2 N/A N/A No information
Spastic paraplegia 4, autosomal dominant N/A N/A No information
Charcot-Marie-Tooth disease, X-linked recessive, 3 N/A N/A No information
Spastic paraplegia 8, autosomal dominant N/A N/A No information
Spastic paraplegia 9, autosomal dominant N/A N/A No information
Charcot-Marie-Tooth disease, Type 2AII N/A N/A No information
Charcot-Marie-Tooth disease, Type 1A N/A N/A No information
Charcot-Marie-Tooth disease, Type 1B N/A N/A No information
Charcot-Marie-Tooth disease, Type 2B N/A N/A No information
Charcot-Marie-Tooth disease, Type 1C N/A N/A No information
Charcot-Marie-Tooth disease, Type 4A N/A N/A No information
Charcot-Marie-Tooth disease, Type 2C N/A N/A No information
Charcot-Marie-Tooth disease, Type 1D N/A N/A No information
Charcot-Marie-Tooth disease, Type 2D N/A N/A No information
Charcot-Marie-Tooth disease, Type 1E N/A N/A No information
Charcot-Marie-Tooth disease, Type 4C N/A N/A No information
Charcot-Marie-Tooth disease, Type 2E N/A N/A No information
Charcot-Marie-Tooth disease, Type 1F N/A N/A No information
Charcot-Marie-Tooth disease, Type 2G N/A N/A No information
Charcot-Marie-Tooth disease, Type 4E N/A N/A No information
Charcot-Marie-Tooth disease, Type 4F N/A N/A No information
Charcot-Marie-Tooth disease, Type 2H N/A N/A No information
Charcot-Marie-Tooth disease, Type 4G N/A N/A No information
Spastic paraplegia type 5A, recessive N/A N/A No information
Charcot-Marie-Tooth disease, Type 2I N/A N/A No information
Charcot-Marie-Tooth disease, Type 4H N/A N/A No information
Spastic paraplegia type 5B, recessive N/A N/A No information
Charcot-Marie-Tooth disease, Type 2J N/A N/A No information
Charcot-Marie-Tooth disease, type 2 N/A N/A No information
Charcot-Marie-Tooth disease, Type 2A N/A N/A No information
Charcot-Marie-Tooth disease, type 4 N/A N/A No information
Charcot-Marie-Tooth disease, demyelinating, autosomal dominant N/A N/A No information
Charcot-Marie-Tooth, demyelinating, autosomal recessive N/A N/A No information
Charcot-Marie-Tooth disease, X-linked N/A N/A No information
Charcot-Marie-Tooth disease, type 1 N/A N/A No information
Charcot-Marie-Tooth disease, Type 2L N/A N/A No information
Spinocerebellar ataxia 11 N/A N/A No information
Spinocerebellar ataxia 20 N/A N/A No information
Spinocerebellar ataxia 12 N/A N/A No information
Spinocerebellar ataxia 21 N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 1 N/A N/A No information
Spinocerebellar ataxia 13 N/A N/A No information
Spinocerebellar ataxia 22 N/A N/A No information
Spinocerebellar ataxia 14 N/A N/A No information
Spinocerebellar ataxia 23 N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 3 N/A N/A No information
Spinocerebellar ataxia 15 N/A N/A No information
Spastic paraplegia 24 N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 5 N/A N/A No information
Spinocerebellar ataxia 17 N/A N/A No information
Spinocerebellar ataxia 26 N/A N/A No information
Absolute Glaucoma N/A N/A No information
Infantile Glaucoma N/A N/A No information
Juvenile Glaucoma N/A N/A No information
Psuedoexfoliative Glaucoma N/A N/A No information
Steroid induced glaucoma. N/A N/A No information
Uveitic Glaucoma N/A N/A No information
Phacomorphic Glaucoma N/A N/A No information
Phacolytic Glaucoma N/A N/A No information
Inflammatory Glaucoma N/A N/A No information
Traumatic Glaucoma N/A N/A No information
Glaucoma in phacomatoses N/A N/A No information
Ghost cell glaucoma N/A N/A No information
Glaucoma in Intra ocular tumours N/A N/A No information
Glaucoma in ciliochorodial detachment N/A N/A No information
Glaucoma in epithelial ingrowth N/A N/A No information
Glaucoma in iridoschisis. N/A N/A No information
Malignant glaucoma N/A N/A No information
Acute Angle Closure Glaucoma N/A N/A No information
Chronic angle closure glaucoma N/A N/A No information
Sub acute angle closure Glaucoma N/A N/A No information
Eye allergy N/A N/A No information
Primary open angle glaucoma N/A N/A No information
Primary angle closure glaucoma N/A N/A No information
Mixed or Combined mechanism Glaucoma N/A N/A No information
Mental retardation -- epilepsy, X-linked N/A N/A No information
Glaucoma N/A N/A No information
Diabetic Peripheral Neuropathy N/A N/A No information
Nerve conditions N/A N/A No information
Brain conditions N/A N/A No information
ADD N/A N/A No information
ADHD N/A N/A No information
Attention Deficit Hyperactivity Disorder N/A N/A No information
Adult ADHD N/A N/A No information
Adult ADD N/A N/A No information
Inattentive ADHD N/A N/A No information
Hyperactive-impulsive ADHD N/A N/A No information
Combined ADHD N/A N/A No information
Residual ADHD N/A N/A No information
Prion diseases N/A N/A No information
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 7 N/A N/A No information
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 6 N/A N/A No information
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 5 N/A N/A No information
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 4 N/A N/A No information
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 3 N/A N/A No information
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 2 N/A N/A No information
Attention Deficit-Hyperactivity Disorder, Susceptibility to, 1 N/A N/A No information
Epilepsy, Childhood Absence, Susceptibility to, 1 N/A N/A No information
Epilepsy, Childhood Absence, Susceptibility to, 2 N/A N/A No information
Epilepsy, Childhood Absence, Susceptibility to, 3 N/A N/A No information
Epilepsy, Childhood Absence, Susceptibility to, 4 N/A N/A No information
Epilepsy, Childhood Absence, Susceptibility to, 5 N/A N/A No information
Epilepsy, Childhood Absence, Susceptibility to, 6 N/A N/A No information
Epilepsy, Juvenile Absence, Susceptibility to, 1 N/A N/A No information
Epilepsy, Juvenile Absence, Susceptibility to, 2 N/A N/A No information
Epilepsy, Juvenile Myoclonic, Susceptibility to, 1 N/A N/A No information
Epilepsy, Juvenile Myoclonic, Susceptibility to, 2 N/A N/A No information
Epilepsy, Juvenile Myoclonic, Susceptibility to, 3 N/A N/A No information
Epilepsy, Juvenile Myoclonic, Susceptibility to, 4 N/A N/A No information
Epilepsy, Juvenile Myoclonic, Susceptibility to, 5 N/A N/A No information
Epilepsy, Juvenile Myoclonic, Susceptibility to, 6 N/A N/A No information
Epilepsy, Juvenile Myoclonic, Susceptibility to, 7 N/A N/A No information
Epilepsy, Juvenile Myoclonic, Susceptibility to, 8 N/A N/A No information
Epilepsy, Idiopathic Generalized, Susceptibility to, 11 N/A N/A No information
Epilepsy, Idiopathic Generalized, Susceptibility to, 7 N/A N/A No information
Epilepsy, Idiopathic Generalized, Susceptibility to, 10 N/A N/A No information
Epilepsy, Idiopathic Generalized, Susceptibility to, 9 N/A N/A No information
Epilepsy, Idiopathic Generalized, Susceptibility to, 8 N/A N/A No information
Polymicrogyria, Bilateral Parasagittal Parieto-Occipital N/A N/A No information
Polymicrogyria, Bilateral Generalized N/A N/A No information
Polymicrogyria, Bilateral Frontal N/A N/A No information
Polymicrogyria, Asymmetric N/A N/A No information
Polymicrogyria, Bilateral Frontoparietal N/A N/A No information
Polymicrogyria N/A N/A No information
Bilateral Occipital Polymicrogyria N/A N/A No information
Schizencephaly N/A N/A No information
Lissencephaly N/A N/A No information
Agyria N/A N/A No information
Macrogyria N/A N/A No information
Pachygyria N/A N/A No information
Progressive Spinobulbar muscular atrophy N/A N/A No information
Kennedy Syndrome N/A N/A No information
Spinal Muscular Atrophy N/A N/A No information
Spinal Muscular Atrophy type I N/A N/A No information
Spinal Muscular Atrophy type II N/A N/A No information
Spinal Muscular Atrophy type III N/A N/A No information
Adult SMA N/A N/A No information
Duchenne Muscular Dystrophy approx 1 in 6,000 or 0.02% or 45,333 people in USA 45,333 about 1 in 3000 males1.
Becker Muscular Dystrophy N/A N/A No information
Muscular dystrophy, Duchenne and Becker type N/A N/A No information
Adult progressive spinal muscular atrophy, Aran Duchenne type N/A N/A No information
Spinocerebellar ataxia 2 N/A N/A No information
Spinocerebellar ataxia 4 N/A N/A No information
Spinocerebellar ataxia 5 N/A N/A No information
Syphilitic aseptic meningitis N/A N/A No information
Spinocerebellar ataxia, Machado-Joseph type I N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 4 N/A N/A No information
Nystagmus, hereditary vertical N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 5 N/A N/A No information
Myasthenia, Limb-Girdle, with Tubular Aggregates N/A N/A No information
Parkinson's disease dementia, familial N/A N/A No information
Primary Parkinsonism N/A N/A No information
Genetic Parkinson disease N/A N/A No information
Parkinson disease, genetic types N/A N/A No information
Parkinson disease 4, autosomal dominant, Lewy body N/A N/A No information
Optic nerve hypoplasia, familial bilateral N/A N/A No information
Parkinson disease 7, autosomal recessive, early-onset N/A N/A No information
Seizures, benign familial neonatal, recessive form N/A N/A No information
Dystonia musculorum deformans type 1 N/A N/A No information
Spinocerebellar ataxia, X-linked, 2 N/A N/A No information
Spastic paraplegia 2, X-linked N/A N/A No information
Dystonia musculorum deformans type 2 N/A N/A No information
Spinocerebellar ataxia, X-linked, 3 N/A N/A No information
Restless Legs Syndrome, Susceptibility To, 7 N/A N/A No information
Restless Legs Syndrome, Susceptibility To, 6 N/A N/A No information
Restless Legs Syndrome, Susceptibility To, 5 N/A N/A No information
Restless Legs Syndrome, Susceptibility To, 4 N/A N/A No information
Restless Legs Syndrome, Susceptibility To, 3 N/A N/A No information
Restless Legs Syndrome, Susceptibility To, 2 N/A N/A No information
Restless Legs Syndrome, Susceptibility To, 1 N/A N/A No information
Alzheimer's Disease N/A N/A No information
Epilepsy approx 1 in 1,502 or 0.07% or 181,000 people in USA 180,999 181,000 people diagnosed each year (CDC)
Optic Atrophy 4 N/A N/A No information
Optic Atrophy 3, Autosomal Dominant N/A N/A No information
Optic Atrophy 7 N/A N/A No information
Optic atrophy 1 N/A N/A No information
Optic atrophy, idiopathic, autosomal recessive N/A N/A No information
Optic atrophy 2 N/A N/A No information
Optic atrophy 5 N/A N/A No information
Lymphedema, microcephaly and chorioretinopathy syndrome N/A N/A No information
Optic atrophy 6 N/A N/A No information
Charcot-Marie-Tooth disease, X-linked, 1 N/A N/A No information
Optic atrophy 1 and deafness N/A N/A No information
Optic atrophy, autosomal dominant N/A N/A No information
Proximal tubulopathy -- diabetes mellitus -- cerebellar ataxia N/A N/A No information
Optic atrophy and cataract, autosomal dominant N/A N/A No information
Ophtalmoplegia myalgia tubular aggregates N/A N/A No information
Opthalmoplegia progressive external scoliosis N/A N/A No information
Deafness, X-Linked 4, Sensorineural Congenital N/A N/A No information
Deafness, X-Linked 2, Sensorineural Congenital N/A N/A No information
Proximal spinal muscular atrophy, type IV N/A N/A No information
Spinal muscular atrophy, Adult form N/A N/A No information
Parkinson disease 7, autosomal recessive early-onset (PARK7) N/A N/A No information
Parkinson disease 4, autosomal dominant Lewy body (PARK4) N/A N/A No information
Parkinson disease 11 (PARK11) N/A N/A No information
Parkinson disease 13 (PARK13) N/A N/A No information
Parkinson disease 5 (PARK5) N/A N/A No information
Parkinson disease 9 (PARK9) N/A N/A No information
Familial Forms of Alzheimer's Disease N/A N/A No information
Alzheimer disease, familial, 4 N/A N/A No information
Alzheimer disease, familial, 11 N/A N/A No information
Alzheimer disease 3, (early-onset Alzheimer disease) N/A N/A No information
Alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques N/A N/A No information
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia N/A N/A No information
Alzheimer disease, early-onset, with cerebral amyloid angiopathy N/A N/A No information
Alzheimer disease 16 N/A N/A No information
Right parietal lobe syndrome related Alzheimer's disease N/A N/A No information
Alzheimer disease 2, late-onset N/A N/A No information
Late-onset Alzheimer's N/A N/A No information
Early-onset Alzheimer's N/A N/A No information
Idiopathic Parkinson's disease N/A N/A No information
Parkinson disease, familial, type 1 (PARK1) N/A N/A No information
Parkinson disease 6, autosomal recessive early-onset (PARK6) N/A N/A No information
Parkinson disease 2, autosomal recessive juvenile (PARK2) N/A N/A No information
Parkinson disease 10 (PARK10) N/A N/A No information
Parkinson disease 12 (PARK12) N/A N/A No information
Parkinson disease 8 (PARK8) N/A N/A No information
Parkinson disease 3, autosomal dominant Lewy body (PARK3) N/A N/A No information
Mitochondrial Parkinson's disease N/A N/A No information
Neurogenic bladder N/A N/A No information
Bell's Palsy approx 1 in 6,800 or 0.01% or 40,000 people in USA 40,000 40,000 annual cases in Americans
Neuritis N/A N/A No information
Trigeminal neuralgia N/A N/A No information
Polyneuritis N/A N/A No information
Peripheral neuritis N/A N/A No information
Cranial neuralgia N/A N/A No information
Postherpetic neuralgia N/A N/A No information
Glossopharyngeal neuralgia N/A N/A No information
Parkinson's Disease N/A N/A No information
Meningitis approx 1 in 10,879 or 0.01% or 25,000 people in USA 25,000 approximately 25,000 cases of bacterial meningitis annually in USA; 206 annual cases in Victoria 1996 (DHS-VIC)
Bacterial meningitis N/A N/A No information
Pneumococcal meningitis approx 1 in 100,000 or 0.00% or 2,720 people in USA 2,720 about 1 to 2 per 100,000 in the USA
Fungal meningitis N/A N/A No information
Leptomeningitis N/A N/A No information
Encephalitis N/A N/A No information
Japanese encephalitis approx 1 in 272,000,000 or 0.00% or 1 people in USA 1 1 case annually in USA (DVBID)
Murray Valley encephalitis N/A N/A No information
Narcolepsy N/A N/A No information
Central sleep apnea N/A N/A No information
Sciatica N/A N/A No information
Spinal cord injury N/A N/A No information
Spinal Cord Disorders N/A N/A No information
Paralysis N/A N/A No information
Paraplegia N/A N/A No information
Neuropathic pain N/A N/A No information
Nervous system disorders N/A N/A No information
Encephalitis, California serogroup viral approx 1 in 3,885,714 or 0.00% or 70 people in USA 70 70 annual cases notified in USA 1999 (MMWR 1999)
Eastern equine encephalitis approx 1 in 54,400,000 or 0.00% or 5 people in USA 5 5 annual cases notified in USA 1999 (MMWR 1999)
St. Louis encephalitis approx 1 in 68,000,000 or 0.00% or 4 people in USA 4 4 annual cases notified in USA 1999 (MMWR 1999)
Western equine encephalitis approx 1 in 272,000,000 or 0.00% or 1 people in USA 1 1 annual cases notified in USA 1999 (MMWR 1999)
Convulsions N/A N/A No information
Opththalmoplegia N/A N/A No information
Optic neuritis N/A N/A No information
Nerve cancer N/A N/A No information
Spinal Cord Tumor N/A N/A No information
Hemangioblastoma N/A N/A No information
Astrocytoma N/A N/A No information
Narcolepsy 5 N/A N/A No information
Narcolepsy 4 N/A N/A No information
Narcolepsy 3 N/A N/A No information
Narcolepsy 2 N/A N/A No information
Narcolepsy 1 N/A N/A No information
Multiple Sclerosis, Susceptibility To, 1 N/A N/A No information
Multiple Sclerosis, Susceptibility To, 2 N/A N/A No information
Multiple Sclerosis, Susceptibility To, 3 N/A N/A No information
Multiple Sclerosis, Susceptibility To, 4 N/A N/A No information
Neuroblastoma, Susceptibility to N/A N/A No information
Hypomyelination, Global Cerebral N/A N/A No information
Leprosy, susceptibility to, 4 N/A N/A No information
Leprosy, susceptibility to, 3 N/A N/A No information
Leprosy, susceptibility to, 2 N/A N/A No information
Leprosy, susceptibility to, 1 N/A N/A No information
Joubert Syndrome 10 N/A N/A No information
Joubert Syndrome 9 N/A N/A No information
Joubert Syndrome 8 N/A N/A No information
Joubert Syndrome 7 N/A N/A No information
Joubert Syndrome 6 N/A N/A No information
Joubert Syndrome 5 N/A N/A No information
Joubert Syndrome 4 N/A N/A No information
Joubert Syndrome 3 N/A N/A No information
Joubert Syndrome 2 N/A N/A No information
Joubert Syndrome 1 N/A N/A No information
Amyotrophic lateral sclerosis, 11 N/A N/A No information
Convulsions, benign familial infantile, 3 N/A N/A No information
Convulsions, benign familial infantile, 4 N/A N/A No information
Congenital Analgesia N/A N/A No information
Congenital Pain Insensitivity N/A N/A No information
Congenital Insensitivity to Pain N/A N/A No information
Congenital Analgesia, Autosomal dominant N/A N/A No information
Congenital indifference to pain, autosomal dominant N/A N/A No information
Indifference to Pain, Congenital, Autosomal Dominant N/A N/A No information
Asymbolia for pain N/A N/A No information
Congenital Analgesia, Autosomal Recessive N/A N/A No information
Congenital indifference to pain, autosomal recessive N/A N/A No information
Indifference to Pain, Congenital, Autosomal Recessive N/A N/A No information
Hypoactive deep tendon reflexes N/A N/A No information
Hyperreflexia N/A N/A No information
Hyperreflexia in children N/A N/A No information
Autosomal recessive spastic paraplegia, type 11 N/A N/A No information
Decreased reflex response N/A N/A No information
Decreased reflexes N/A N/A No information
Decreased pain sensation N/A N/A No information
Decreased penile sensation N/A N/A No information
Charcot-Marie-Tooth disease (generic term) N/A N/A No information
Primary dystonia N/A N/A No information
Subacute sclerosing leukoencephalitis N/A N/A No information
Senile Retinoschisis N/A N/A No information
Retinoschisis, X-linked N/A N/A No information
Colourblindness, tritan N/A N/A No information
Retinoschisis, juvenile N/A N/A No information
Colorblindness, tritanopic N/A N/A No information
Juvenile Retinoschisis N/A N/A No information
Blue colourblindness N/A N/A No information
Juvenile Myasthenia Gravis N/A N/A No information
Congenital Myasthenia Gravis N/A N/A No information
Transient Neonatal Myasthenia Gravis N/A N/A No information
Generalized Myasthenia Gravis N/A N/A No information
Ocular Myasthenia Gravis N/A N/A No information
Myasthenia, Familial Infantile, 1 N/A N/A No information
Myasthenia Gravis with Thymus Hyperplasia N/A N/A No information
Myasthenia, Congenital, Refractory to Acetylcholinesterase Inhibitors N/A N/A No information
Pontocerebellar Hypoplasia Type 2C N/A N/A No information
Pontocerebellar Hypoplasia Type 2B N/A N/A No information
Pontocerebellar Hypoplasia Type 6 N/A N/A No information
Fetal-onset olivopontocerebellar hypoplasia N/A N/A No information
Pontocerebellar hypoplasia type V N/A N/A No information
Primary restless leg syndrome N/A N/A No information
Secondary restless leg syndrome N/A N/A No information
Neurological chronic fatigue syndrome N/A N/A No information
Post-ADD chronic fatigue syndrome N/A N/A No information
Post-viral CFS N/A N/A No information
Infectious CFS N/A N/A No information
Musculoskeletal chronic fatigue syndrome N/A N/A No information
CFS subtype 7 (pain, infectious, musculoskeletal, sleep, neurological, gastrointestinal, neurocognitive, anxiety/depression) N/A N/A No information
CFS subtype 6 (postexertional) N/A N/A No information
CFS subtype 5 (musculoskeletal, gastrointestinal) N/A N/A No information
CFS subtype 4 (cognitive, musculoskeletal, sleep, anxiety/depression) N/A N/A No information
CFS subtype 3 (mild) N/A N/A No information
CFS subtype 2 ( musculoskeletal, pain, anxiety/depression) N/A N/A No information
CFS subtype 1 (cognitive, musculoskeletal, sleep, anxiety/depression) N/A N/A No information
Deposition diseases related fibromyalgia N/A N/A No information
Tension myositis related fibromyalgia N/A N/A No information
Sleep disturbance related fibromyalgia N/A N/A No information
Major depressive disorder related fibromyalgia N/A N/A No information
SLE related fibromyalgia N/A N/A No information
Rheumatoid arthritis related fibromyalgia N/A N/A No information
Epstein Barr virus related fibromyalgia N/A N/A No information
Secondary Fibromyalgia N/A N/A No information
Primary Fibromyalgia N/A N/A No information
Neuralgia pain N/A N/A No information
Phantom limb pain N/A N/A No information
Contralateral athetosis N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 43 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 25 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 44 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 53 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 17 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 36 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 18 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 47 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 28 N/A N/A No information
Amyotrophic lateral sclerosis approx 1 in 54,400 or 0.00% or 5,000 people in USA 5,000 estimated 5,000 people are diagnosed with amyotrophic lateral sclerosis in the US, Genetics Home Reference website
Myasthenia Gravis N/A N/A No information
Neonatal myasthenia N/A N/A No information
Wilson's Disease N/A N/A No information
Encephaloceles approx 1 in 400,000 or 0.00% or 680 people in USA 680 1.7 per 10,000 births in the UK 2002 for encephalocele (University of Ulster, 2003)
Neurodermatitis N/A N/A No information
Fibromyalgia N/A N/A No information
Traumatic Brain Injury approx 1 in 858 or 0.12% or 316,785 people in USA 316,785 9,484 in NJ 1997 (NJ DHSS)
Tremor N/A N/A No information
Essential tremor N/A N/A No information
Orthostatic tremor N/A N/A No information
Tropical Spastic Paraparesis N/A N/A No information
Benign Multiple Sclerosis N/A N/A No information
Relapsing/remitting multiple sclerosis N/A N/A No information
Secondary chronic progressive multiple sclerosis N/A N/A No information
Primary progressive multiple sclerosis N/A N/A No information
Marburg multiple sclerosis N/A N/A No information
Optic-spinal form of multiple sclerosis N/A N/A No information
Nerve entrapment N/A N/A No information
Pudendal nerve entrapment N/A N/A No information
Acute meningitis N/A N/A No information
Eosinophilic meningitis N/A N/A No information
Anthrax meningitis N/A N/A No information
Chronic meningitis N/A N/A No information
Recurring meningitis N/A N/A No information
Chemical meningitis N/A N/A No information
Carcinomatous meningitis N/A N/A No information
Meningococcal A N/A N/A No information
Meningococcal B N/A N/A No information
Meningococcal C N/A N/A No information
Infectious meningitis N/A N/A No information
Tuberous sclerosis N/A N/A No information
Guillain-Barre Syndrome approx 1 in 100,000 or 0.00% or 2,720 people in USA 2,720 about 1 in 100,000 (NWHIC)
Balo disease N/A N/A No information
Autoimmune Myelopathy N/A N/A No information
Chronic Fatigue Syndrome N/A N/A No information
Shingles approx 1 in 544 or 0.18% or 500,000 people in USA 499,999 500,000 cases (NIAID)
Lyme disease approx 1 in 2,719 or 0.04% or 100,000 people in USA 100,000 estimated 100,000 cases annually (NIAID/USA)
Normal Pressure Hydrocephalus N/A N/A No information
Oculomotor Migraine N/A N/A No information
Spastic paraparesis N/A N/A No information
Basilar Migraine N/A N/A No information
Ulnar Neuropathy N/A N/A No information
Encephalocele frontal N/A N/A No information
Iniencephaly N/A N/A No information
Primary angiitis of the central nervous system N/A N/A No information
Neuropathy N/A N/A No information
Diabetic neuropathy N/A N/A No information
Peripheral neuropathy N/A N/A No information
Hand neuropathy N/A N/A No information
Autonomic neuropathy N/A N/A No information
Sexual neuropathy N/A N/A No information
Eye neuropathy N/A N/A No information
Vascular neuropathy N/A N/A No information
Radiculopathy N/A N/A No information
Mental retardation, keratoconus, febrile seizures, and sinoatrial block N/A N/A No information
Autonomic nerve disorders N/A N/A No information
Dysautonomia N/A N/A No information
Multiple Sclerosis N/A N/A No information
Autoimmune neuropathies N/A N/A No information
Dementia approx 1 in 738 or 0.14% or 368,320 people in USA 368,320 6,175 annual cases in Victora 1996 (DHS-VIC)
Multi-Infarct Dementia N/A N/A No information
Dementia With Lewy Bodies N/A N/A No information
Myoclonus N/A N/A No information
Chorea N/A N/A No information
Sydenham chorea N/A N/A No information
Acute Disseminated Encephalomyelitis N/A N/A No information
Leukodystrophy N/A N/A No information
Adrenoleukodystrophy N/A N/A No information
Classic childhood ALD N/A N/A No information
Adult-onset ALD N/A N/A No information
Female carrier ALD N/A N/A No information
Neonatal ALD N/A N/A No information
Agnosia N/A N/A No information
Arachnoiditis N/A N/A No information
Arachnoid Cysts N/A N/A No information
Batten Disease N/A N/A No information
Ceroid lipofuscinosis, neuronal 3, Juvenile N/A N/A No information
Ceroid lipofuscinosis, neuronal 4 N/A N/A No information
Ceroid lipofuscinosis, neuronal 6, late infantile N/A N/A No information
Ceroid lipofuscinosis, neuronal 8, northern epilepsy variant N/A N/A No information
Ceroid lipofuscinosis, neuronal 5 N/A N/A No information
Ceroid lipofuscinosis, neuronal 7 N/A N/A No information
Ceroid lipofuscinosis, neuronal 8 N/A N/A No information
Ceroid lipofuscinosis, neuronal 9 N/A N/A No information
Ceroid lipofuscinosis, neuronal 10 N/A N/A No information
Ceroid lipofuscinosis, neuronal N/A N/A No information
Ceroid lipofuscinosis, neuronal 1, infantile N/A N/A No information
Ceroid lipofuscinosis, neuronal 2, late infantile type N/A N/A No information
Santavuori Disease N/A N/A No information
Bielschowsky disease N/A N/A No information
Primary Lateral Sclerosis N/A N/A No information
Progressive Multifocal Leukoencephalopathy N/A N/A No information
Progressive Supranuclear Palsy N/A N/A No information
Rasmussen's Encephalitis N/A N/A No information
Refsum Disease N/A N/A No information
Restless Legs Syndrome N/A N/A No information
Periodic limb movements in sleep N/A N/A No information
Pinched Nerve N/A N/A No information
Headache-free migraine N/A N/A No information
Multifocal motor neuropathy N/A N/A No information
Charcot-Marie-Tooth disease, X-linked recessive, 4 N/A N/A No information
Spastic paraplegia 6, autosomal dominant N/A N/A No information
Charcot-Marie-Tooth disease, X-linked recessive, 5 N/A N/A No information
Ehlers-Danlos syndrome with periventricular heterotopia N/A N/A No information
Microlissencephaly N/A N/A No information
Microlissencephaly -- micromelia N/A N/A No information
Microphthalmia -- brain atrophy N/A N/A No information
Sixth nerve palsy N/A N/A No information
Shock, Neurogenic N/A N/A No information
Paresis N/A N/A No information
Catamenial seizure N/A N/A No information
Anosognosia N/A N/A No information
Radial Nerve Entrapment N/A N/A No information
Gelastic seizure N/A N/A No information
Anterior Interosseous Nerve Compression N/A N/A No information
Atonic seizure N/A N/A No information
Brachioradial pruritus N/A N/A No information
Focal emotional seizure N/A N/A No information
Secondarily generalized seizure N/A N/A No information
Startle epilepsy N/A N/A No information
Focal motor seizure N/A N/A No information
Olefactory seizure N/A N/A No information
Posterior Interosseous Nerve Syndrome N/A N/A No information
Visual seizure N/A N/A No information
Partial emotional seizure N/A N/A No information
Complex partial seizure N/A N/A No information
Myoclonic seizures N/A N/A No information
Alcoholic polyneuropathy N/A N/A No information
Vestibular seizure N/A N/A No information
Focal sensory seizure N/A N/A No information
Psychic simple partial seizure N/A N/A No information
Partial motor seizure N/A N/A No information
Partial sensory seizure N/A N/A No information
Guyon tunnel syndrome N/A N/A No information
Focal somatosensory seizure N/A N/A No information
Partial somatosensory seizure N/A N/A No information
Autosomal dominant nocturnal frontal lobe epilepsy N/A N/A No information
Absence seizure N/A N/A No information
Abdominal seizure N/A N/A No information
Focal seizure N/A N/A No information
Rolandic Epilepsy N/A N/A No information
Abdominal nerve entrapment N/A N/A No information
Anterior Interosseous Nerve Syndrome N/A N/A No information
Clonic seizures N/A N/A No information
Tonic-Clonic seizure N/A N/A No information
Tonic seizure N/A N/A No information
Emotional seizure N/A N/A No information
Nerve compression N/A N/A No information
Autonomic seizure N/A N/A No information
Simple partial seizure N/A N/A No information
Sensory nerve trauma N/A N/A No information
Sensory seizure N/A N/A No information
Partial seizure N/A N/A No information
Upper motor neuron lesions like hyperactive DTRs in the legs N/A N/A No information
Hepatic encephalopathy like coma N/A N/A No information
Bilateral stroke N/A N/A No information
Meningitis-like neck stiffness N/A N/A No information
Glaucoma associated with systemic abnormalities N/A N/A No information
HIV-like dysguesia N/A N/A No information
Glaucoma-like clouding of vision N/A N/A No information
Neurological disorders related to AIDS N/A N/A No information
Stroke-like dysarthria N/A N/A No information
Glaucoma acquired secondary to intraocular neoplasm N/A N/A No information
Primary glaucoma associated with ocular abnormalities N/A N/A No information
Alcoholic cerebellar degeneration N/A N/A No information
Facial paresthesia N/A N/A No information
Stroke-like aphasia N/A N/A No information
Tactile hallucinations N/A N/A No information
Variable sensory loss N/A N/A No information
Hypnagogic hallucinations N/A N/A No information
Colored haloes similar to that of glaucoma N/A N/A No information
Tingling sensation down the neck N/A N/A No information
Extraocular muscle palsies N/A N/A No information
Diabetes-like neuropathy symptoms N/A N/A No information
Hemiballismus N/A N/A No information
Choreoathetosis N/A N/A No information
Sensory ataxia N/A N/A No information
Sciatica as seen in rheumatoid arthritis N/A N/A No information
Drop attacks as seen in stroke N/A N/A No information
Restless leg syndrome N/A N/A No information
Oculomotor palsy N/A N/A No information
Choreiform movements as seen in rheumatic fever N/A N/A No information
Carcinomatous polyneuropathy N/A N/A No information
Rheumatic fever-like chorea N/A N/A No information
Myelomatous polyneuropathy N/A N/A No information
Uremic encephalopathy N/A N/A No information
Gullian-Barre-like hyporeflexia N/A N/A No information
Brain stem lesions N/A N/A No information
Recurring headache N/A N/A No information
Hereditary Congenital Facial Paresis II N/A N/A No information
Hereditary Congenital Facial Paresis 2 N/A N/A No information
Hereditary Congenital Facial Paresis I N/A N/A No information
Hereditary Congenital Facial Paresis N/A N/A No information
Pfeiffer Syndrome Type II N/A N/A No information
Pfeiffer Syndrome Type III N/A N/A No information
Acrocephalosyndactyly Syndrome type 5 N/A N/A No information
Acrocephalosyndactyly type 5 (ACPS 5) N/A N/A No information
Pfeiffer syndrome N/A N/A No information
Pfeiffer syndrome Type 2 N/A N/A No information
Pfeiffer syndrome Type 3 N/A N/A No information
Absence of septum pellucidum N/A N/A No information
Aicardi-Goutieres syndrome 1 N/A N/A No information
Aicardi-Goutieres syndrome 2 N/A N/A No information
Aicardi-Goutieres syndrome 3 N/A N/A No information
Aicardi syndrome N/A N/A No information
Aicardi-Goutieres syndrome 4 N/A N/A No information
Pseudo-torch syndrome N/A N/A No information
Aicardi-Goutieres syndrome N/A N/A No information
Aicardi-Goutieres syndrome 5 N/A N/A No information
Ehlers-Danlos syndrome, progeroid form 2 N/A N/A No information
Charcot-Marie-Tooth disease -- deafness N/A N/A No information
Charcot-Marie-Tooth Disorder N/A N/A No information
Charcot disease N/A N/A No information
Charcot-Marie-Tooth disease, Type 2K N/A N/A No information
Charcot-Marie-Tooth disease with ptosis and parkinsonism N/A N/A No information
Charcot-Marie-Tooth type 1 aplasia cutis congenital N/A N/A No information
Torsion dystonia 7 N/A N/A No information
Primary open angle glaucoma juvenile onset 1 N/A N/A No information
Charcot-Marie-Tooth disease, Type 2B1 N/A N/A No information
Charcot-Marie-Tooth disease, Type 2B2 N/A N/A No information
Charcot-Marie-Tooth disease, Type 4B1 N/A N/A No information
Charcot-Marie-Tooth disease, Type 4B2 N/A N/A No information
Charcot-Marie-Tooth disease, Type 2AI N/A N/A No information
Charcot-Marie-Tooth disease, dominant intermediate 1 N/A N/A No information
Charcot-Marie-Tooth disease, dominant intermediate 2 N/A N/A No information
Charcot-Marie-Tooth disease, dominant intermediate 3 N/A N/A No information
Spastic paraplegia type 1, X-linked N/A N/A No information
Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma N/A N/A No information
Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant N/A N/A No information
Charcot-Marie-Tooth disease deafness recessive type N/A N/A No information
Charcot-Marie-Tooth disease, Type 2F N/A N/A No information
Autosomal Dominant Charcot-Marie-Tooth with hearing loss N/A N/A No information
Spastic Paraplegia 18, Autosomal Recessive N/A N/A No information
Spastic paraplegia 11, autosomal recessive N/A N/A No information
Spastic paraplegia 23 N/A N/A No information
Spastic paraplegia 17 N/A N/A No information
Spastic paraplegia 20, autosomal recessive N/A N/A No information
Spastic paraplegia 14, autosomal recessive N/A N/A No information
Spastic paraplegia 15, autosomal recessive N/A N/A No information
Spastic paraplegia 25, autosomal recessive N/A N/A No information
Spastic paraplegia 26, autosomal recessive N/A N/A No information
Spastic paraplegia 16, X-linked N/A N/A No information
Spastic paraplegia 10, autosomal dominant N/A N/A No information
Spastic paraplegia 12, autosomal dominant N/A N/A No information
Spastic paraplegia 13, autosomal dominant N/A N/A No information
Spastic paraplegia 19, autosomal dominant N/A N/A No information
Spastic paraplegia 29, autosomal dominant N/A N/A No information
Spastic paraplegia 7, autosomal recessive N/A N/A No information
Spastic paraplegia 39, autosomal recessive N/A N/A No information
Spastic paraplegia 31, autosomal dominant N/A N/A No information
Chiari Malformation N/A N/A No information
Chiari-1 Malformation N/A N/A No information
Arnold-Chiari Malformation (Type 1) N/A N/A No information
Arnold-Chiari Syndrome N/A N/A No information
Arnold-Chiari malformation type 2 N/A N/A No information
Arnold-Chiari malformation type 3 N/A N/A No information
Arnold-Chiari malformation type 4 N/A N/A No information
Parkinsonism, early onset with mental retardation N/A N/A No information
Mental retardation progressive spasticity, X-linked N/A N/A No information
Cerebral Atrophy N/A N/A No information
Spastic disorders N/A N/A No information
Spasticity N/A N/A No information
Cerebral Palsy approx 1 in 34,000 or 0.00% or 8,000 people in USA 8,000 2 to 2.5 per 1,000 births (FMC)
Amyotrophic lateral sclerosis 7 N/A N/A No information
Amyotrophic lateral sclerosis 8 N/A N/A No information
Amyotrophic lateral sclerosis, 9 N/A N/A No information
Amyotrophic lateral sclerosis 2, juvenile N/A N/A No information
Amyotrophic lateral sclerosis 4, juvenile N/A N/A No information
Amyotrophic lateral sclerosis, type 6 N/A N/A No information
Amyotrophic lateral sclerosis, familial type 1 N/A N/A No information
Amyotrophic lateral sclerosis, familial type 2 N/A N/A No information
Amyotrophic lateral sclerosis, familial type 3 N/A N/A No information
Amyotrophic lateral sclerosis, familial type 4 N/A N/A No information
Amyotrophic lateral sclerosis, familial type 5 N/A N/A No information
Amyotrophic lateral sclerosis, familial type 6 N/A N/A No information
Amyotrophic lateral sclerosis, familial type 7 N/A N/A No information
Amyotrophic lateral sclerosis, familial type 8 N/A N/A No information
Amyotrophic lateral sclerosis, familial N/A N/A No information
Amyotrophic lateral sclerosis type 1 N/A N/A No information
Amyotrophic lateral sclerosis-parkinsonism/dementia complex 2 N/A N/A No information
Amyotrophic lateral sclerosis-parkinsonism-dementia complex N/A N/A No information
Amyotrophic lateral sclerosis 3 N/A N/A No information
Amyotrophic lateral sclerosis 5 N/A N/A No information
Amyotrophic lateral sclerosis 6 N/A N/A No information
AIDS Dementia Complex N/A N/A No information
Neonatal bacterial meningitis N/A N/A No information
Usher syndrome, type 1C N/A N/A No information
Usher syndrome, type 2B N/A N/A No information
Usher syndrome, type 1B N/A N/A No information
Usher syndrome, type 2A N/A N/A No information
Usher syndrome, type 1D N/A N/A No information
Usher syndrome, type 2C N/A N/A No information
Usher syndrome, type 1E N/A N/A No information
Usher syndrome, type 1F N/A N/A No information
Usher syndrome, type IIA N/A N/A No information
Usher syndrome, type IIB N/A N/A No information
Usher syndrome, type IIC N/A N/A No information
Usher syndrome, type 1G N/A N/A No information
Usher syndrome, type IIIA N/A N/A No information
Usher syndrome, type IIIB N/A N/A No information
Usher Syndrome 1H N/A N/A No information
Usher Syndrome N/A N/A No information
Usher Syndrome Type 1 N/A N/A No information
Usher Syndrome Type 2 N/A N/A No information
Usher Syndrome Type 3 N/A N/A No information
Brain abscess N/A N/A No information
Brain compression N/A N/A No information
Brain damage N/A N/A No information
Cephalic disorders N/A N/A No information
Cerebral hemorrhage N/A N/A No information
Delirium N/A N/A No information
Neural tube defect approx 1 in 58,772 or 0.00% or 4,627 people in USA 4,627 11.57 per 10,000 births with neural tube defects in the UK 2002 (University of Ulster, 2003)
Lymphocytic Choriomeningitis N/A N/A No information
Granulomatous amebic encephalitis N/A N/A No information
Naegleria N/A N/A No information
Neurotoxic shellfish poisoning N/A N/A No information
Central nervous system infections N/A N/A No information
Fissures N/A N/A No information
POEMS N/A N/A No information
Vasovagal attack N/A N/A No information
Subarachnoid haemorrhage N/A N/A No information
Catalepsy N/A N/A No information
Erythromelalgia N/A N/A No information
Focal seizures N/A N/A No information
Generalized seizures N/A N/A No information
Akathisia N/A N/A No information
High altitude cerebral edema N/A N/A No information
Herpes zoster oticus N/A N/A No information
Ramsay Hunt syndrome Type II N/A N/A No information
Intercostal neuralgia N/A N/A No information
Transient burning N/A N/A No information
Temporary burning N/A N/A No information
Recurrent headache N/A N/A No information
Mild burning N/A N/A No information
Occasional tremors N/A N/A No information
Mild headache N/A N/A No information
Severe headache N/A N/A No information
Anosmia N/A N/A No information
Post-vaccinial encephalitis N/A N/A No information
Neuroma N/A N/A No information
Myoclonus epilepsy partial seizure N/A N/A No information
Alzheimer disease type 2 N/A N/A No information
Alzheimer disease type 1 N/A N/A No information
Infantile parkinsonism N/A N/A No information
Brain tumor, adult approx 1 in 13,268 or 0.01% or 20,500 people in USA 20,500 estimated 20,500 new cases of brain cancer will be diagnosed in the US in 2007, National Cancer Institute website
Spinocerebellar ataxia 3 N/A N/A No information
Dysmyelination N/A N/A No information
Agenesis of the corpus callosum N/A N/A No information
Anencephaly approx 1 in 68,000 or 0.00% or 4,000 people in USA 4,000 less than 4,000 cases (the rate for spina bifida and anencephaly, NWHIC)
Dandy-Walker Syndrome N/A N/A No information
Empty Sella Syndrome N/A N/A No information
Hydranencephaly N/A N/A No information
Mobius syndrome N/A N/A No information
Neuronal Migration Disorders N/A N/A No information
Holoprosencephaly approx 1 in 285,714 or 0.00% or 951 people in USA 951 2.38 per 10,000 births in the UK 2002 for arhinencephaly/holprosencephaly (University of Ulster, 2003)
Deafness, autosomal dominant nonsyndromic sensorineural 10 N/A N/A No information
Radiation-Induced Brachial Plexopathy N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 11 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 48 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 49 N/A N/A No information
Parkinson disease, juvenile, autosomal recessive N/A N/A No information
Microcephaly -- chorioretinopathy, recessive form N/A N/A No information
Spinal bulbar motor neuropathy N/A N/A No information
Mental retardation, X-linked -- hypogammaglobulinemia -- progressive neurological deterioration N/A N/A No information
Mental retardation, X-linked -- choreoathesis -- abnormal behavior N/A N/A No information
Mental retardation, X-linked -- corpus callosum agenesis -- spastic quadriparesis N/A N/A No information
Mental retardation, X-linked -- epilepsy -- progressive joint contractures -- typical face N/A N/A No information
Diabetes Insipidus, Neurogenic N/A N/A No information
Mental retardation, X-linked -- craniofacial dysmorphology -- epilepsy -- ophthalmoplegia -- cerebellar atrophy N/A N/A No information
Proximal spinal muscular atrophy, type 3 N/A N/A No information
Multiple system atrophy N/A N/A No information
Myoclonic progressive familial epilepsy N/A N/A No information
Parkinson disease, familial, Type 1 N/A N/A No information
Parkinson disease 12 N/A N/A No information
Parkinson disease 13 N/A N/A No information
Deafness, neurosensory nonsyndromic recessive, DFN N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 1 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 2 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 3 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 6 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 7 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 8 N/A N/A No information
Deafness conductive stapedial ear malformation facial palsy N/A N/A No information
Complex partial seizure disorder N/A N/A No information
Immunosuppressive Measles Encephalitis N/A N/A No information
Measles Encephalitis in Children with Immunosuppression N/A N/A No information
Chronic Vilyisk Encephalomyelitis N/A N/A No information
Chronic Vilyuisk Encephalitis N/A N/A No information
Chronic Bokhoror N/A N/A No information
Chronic Viliuisk Encephaliti N/A N/A No information
Chronic Viliuisk Encephalomyelitis N/A N/A No information
Slowly Progressive Viliuisk Encephalomyelitis N/A N/A No information
Slowly Progressive Viliuisk Encephalitis N/A N/A No information
Slowly Progressive VE N/A N/A No information
Slowly Progressive Bokhoror N/A N/A No information
Slowly Progressive Vilyuisk Encephalomyelitis N/A N/A No information
Slowly Progressive Vilyuisk Encephalitis N/A N/A No information
Acute Vilyuisk Encephalitis N/A N/A No information
Acute VE N/A N/A No information
Acute Bokhoror N/A N/A No information
Acute Viliuisk Encephalomyelitis N/A N/A No information
Acute Viliuisk Encephalitis N/A N/A No information
Acute Vilyuisk Encephalomyelitis N/A N/A No information
Parkinsonism, early-onset -- mental retardation N/A N/A No information
Parkinson disease 3 N/A N/A No information
Parkinson disease 9 N/A N/A No information
Parkinson disease 8 N/A N/A No information
Parkinson disease 6, autosomal recessive, recessive early-onset N/A N/A No information
Parkinson disease 10 N/A N/A No information
Parkinson disease 11 N/A N/A No information
Alzheimer disease, familial, 1 N/A N/A No information
Alzheimer disease 5 N/A N/A No information
Alzheimer disease 6 N/A N/A No information
Alzheimer disease 7 N/A N/A No information
Alzheimer disease 8 N/A N/A No information
Alzheimer disease 9 N/A N/A No information
Alzheimer disease 10 N/A N/A No information
Alzheimer disease 12 N/A N/A No information
Permanent brain damage N/A N/A No information
Intellectual handicap N/A N/A No information
Brain infection N/A N/A No information
Dystonia 6, torsion N/A N/A No information
Epilepsy -- telangiectasia N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 2 N/A N/A No information
Facial clefting corpus callosum agenesis N/A N/A No information
Aniridia cerebellar ataxia mental deficiency N/A N/A No information
Vestibular neuritis N/A N/A No information
Extrasystoles -- short stature -- hyperpigmentation -- microcephaly N/A N/A No information
Median cleft lip, corpus callosum, lipoma, and skin polyps N/A N/A No information
Mental retardation, Behavior disturbance, Sensorineural hearing loss N/A N/A No information
Neuropathy motor sensory type 2 deafness mental retardation N/A N/A No information
Hypoplastic thumbs -- hydranencephaly N/A N/A No information
Intracranial aneurysms -- multiple congenital anomaly N/A N/A No information
Tibial aplasia -- ectrodactyly -- hydrocephalus N/A N/A No information
Microcephaly -- cervical spine fusion anomalies N/A N/A No information
Fetal brain disruption sequence N/A N/A No information
Deafness neurosensory -- pituitary dwarfism N/A N/A No information
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy N/A N/A No information
Dandy-Walker malformation postaxial polydactyly N/A N/A No information
Microcephaly -- seizures -- mental retardation -- heart disorders N/A N/A No information
Deafness hyperuricemia neurologic ataxia N/A N/A No information
Facial asymmetry -- temporal seizures N/A N/A No information
Opticoacoustic nerve atrophy dementia N/A N/A No information
Deafness -- Opticoacoustic nerve atrophy -- dementia N/A N/A No information
Deafness, congenital neurosensory, autosomal recessive 10 N/A N/A No information
Deafness, autosomal dominant nonsyndromic sensorineural 9 N/A N/A No information
Microcephaly -- sparse hair -- mental retardation -- seizures N/A N/A No information
Pachygyria -- mental retardation -- seizures N/A N/A No information
Ataxia-oculomotor apraxia syndrome N/A N/A No information
Deafness peripheral -- neuropathy -- arterial disease N/A N/A No information
Spastic paraplegia epilepsy mental retardation N/A N/A No information
Craniosynostosis -- Dandy-Walker -- Hydrocephalus N/A N/A No information
Mental retardation athetosis microphthalmia N/A N/A No information
Mental retardation -- skeletal dysplasia -- abducens palsy N/A N/A No information
Microcephaly with spastic quadriplegia N/A N/A No information
Pontoneocerebellar Hypoplasi N/A N/A No information
Mental retardation -- epilepsy N/A N/A No information
Short stature -- microcephaly -- seizures -- deafness N/A N/A No information
Mental retardation, X-linked -- dystonia -- dysarthria N/A N/A No information
Microcephaly -- mesobrachyphalangy -- tracheoesophageal fistula syndrome N/A N/A No information
Retinopathy -- aplastic anemia -- neurological abnormalities N/A N/A No information
Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance N/A N/A No information
Ataxia spastic congenital miosis N/A N/A No information
Athetosis N/A N/A No information
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate N/A N/A No information
Iris dysplasia with ocular hypertelorism, psychomotor retardation and sensorineural deafness N/A N/A No information
Macrostomia -- preauricular tags -- external ophthalmoplegia N/A N/A No information
Unusual facies, macrocephaly, aplasia of corpus callosum, seizures, hypertrichosis, claw hands and overlapping fingers N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 7 N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 9 N/A N/A No information
Diabetes mellitus, permanent neonatal -- pancreatic and cerebellar agenesis N/A N/A No information
Fronto-temporal dementia and Parkinsonism linked to chromosome 17 (FTDP-17) N/A N/A No information
Serratia meningitis N/A N/A No information
Febrile convulsions, familial, 1 N/A N/A No information
Febrile convulsions, familial, 2 N/A N/A No information
Febrile convulsions, familial, 3 N/A N/A No information
Febrile convulsions, familial, 4 N/A N/A No information
Febrile convulsions, familial, 5 N/A N/A No information
Febrile convulsions, familial, 6 N/A N/A No information
Febrile convulsions, familial, 7 N/A N/A No information
Febrile convulsions, familial, 8 N/A N/A No information
Febrile convulsions, familial, 9 N/A N/A No information
Alzheimer disease 13 N/A N/A No information
Alzheimer disease 14 N/A N/A No information
Basal ganglia calcification, idiopathic 1 N/A N/A No information
Basal ganglia calcification, idiopathic 2 N/A N/A No information
Alzheimer's disease without Neurofibrillary tangles N/A N/A No information
Alzheimer disease, familial, type 3 N/A N/A No information
Alzheimer disease type 4 N/A N/A No information
Alzheimer disease, familial N/A N/A No information
Alzheimer disease 15 N/A N/A No information
Spinocerebellar ataxia 8 N/A N/A No information
Spinocerebellar ataxia, X-linked, 5 N/A N/A No information
Spinocerebellar ataxia -- dysmorphism N/A N/A No information
Spinocerebellar ataxia with axonal neuropathy, type 2 N/A N/A No information
Spinocerebellar ataxia, X-linked, type 4 N/A N/A No information
Spinocerebellar Ataxia 9 N/A N/A No information
Friedreich's ataxia N/A N/A No information
Spinocerebellar Ataxia N/A N/A No information
Progressive external ophthalmoplegia N/A N/A No information
Myoclonus epilepsy N/A N/A No information
Creutzfeldt-Jakob Disease approx 1 in 1,000,000 or 0.00% or 271 people in USA 271 1-per-million
Variant CJD N/A N/A No information
Kuru approx 1 in 0 or 0.00% or 0 people in USA 0 0%; the disease is almost extinct.
Fatal familial insomnia N/A N/A No information
Feline spongiform encephalopathy N/A N/A No information
Bovine spongiform encephalopathy N/A N/A No information
Chronic wasting disease (CWD) of mule deer and elk N/A N/A No information
Transmissible mink encephalopathy (TME) N/A N/A No information
Alternating Hemiplegia N/A N/A No information
Motor neuron diseases approx 1 in 49,566 or 0.00% or 5,487 people in USA 5,487 92 annual cases in Victoria 1996 (DHS-VIC)
Cerebral Aneurysm N/A N/A No information
Dystonias N/A N/A No information
Hereditary Spastic Paraplegia N/A N/A No information
Progressive muscular atrophy N/A N/A No information
Occipital Neuralgia N/A N/A No information
Neuralgia N/A N/A No information
Opsoclonus Myoclonus N/A N/A No information
Paresthesia N/A N/A No information
Primary amoebic meningoencephalitis N/A N/A No information
Mild Traumatic Brain Injury approx 1 in 194 or 0.51% or 1.4 million people in USA 1,400,000 Estimated 1.4 million MTBI injuries per year in the USA (CDC)
Quadriplegia N/A N/A No information
Alcoholic Neuropathy N/A N/A No information
Schwannoma N/A N/A No information
Leukoencephalopathy N/A N/A No information
Autoimmune nerve disorders N/A N/A No information
Listeriosis meningoencephalitis N/A N/A No information
Torsion dystonia, X-linked N/A N/A No information
Rasmussen encephalitis N/A N/A No information
GM2-gangliosidosis, AB variant N/A N/A No information
Neurosyphilis -- general paresis N/A N/A No information
Hereditary spastic paralysis, infantile onset ascending N/A N/A No information
Friedreich ataxia N/A N/A No information
Spinal muscular atrophy, type 3 N/A N/A No information
Spinal muscular atrophy with respiratory distress 1 N/A N/A No information
Spinal muscular atrophy type 2 N/A N/A No information
Spinal muscular atrophy, type I, with congenital bone fractures N/A N/A No information
Spinal muscular atrophy, Ryukyuan type N/A N/A No information
Athetoid Cerebral Palsy N/A N/A No information
Mixed Cerebral Palsy N/A N/A No information
Cerebral Palsy, Ataxic, Autosomal Recessive N/A N/A No information
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy N/A N/A No information
Cerebral Palsy, Spastic Quadriplegic, 1 N/A N/A No information
Cerebral Palsy, Spastic Quadriplegic, 2 N/A N/A No information
Cerebral Palsy, Spastic Quadriplegic, 3 N/A N/A No information
Glaucoma, normal tension, susceptibility to N/A N/A No information
Glaucoma -- iridogoniodysgenesia N/A N/A No information
Glaucoma 1, open angle, G N/A N/A No information
Glaucoma, hereditary N/A N/A No information
Glaucoma, primary open angle N/A N/A No information
Glaucoma 1, open angle C N/A N/A No information
Glaucoma 1, open angle D N/A N/A No information
Glaucoma 1, open angle, E N/A N/A No information
Glaucoma 1, open angle F N/A N/A No information
Glaucoma 1, open angle, I N/A N/A No information
Glaucoma 1, open angle, J N/A N/A No information
Glaucoma 1, open angle, K N/A N/A No information
Glaucoma 3, primary congenital A N/A N/A No information
Glaucoma 3, primary infantile, B N/A N/A No information
Glaucoma -- sleep apnea N/A N/A No information
Glaucoma, congenital N/A N/A No information
Microcephaly -- microphthalmia -- ectrodactyly of lower limbs -- prognathism N/A N/A No information
Neurological causes of muscle weakness N/A N/A No information
Epilepsy-like myoclonic jerks N/A N/A No information
Decerebrate posture as in case of brainstem transection N/A N/A No information
Metabolic encephalopathy N/A N/A No information
Cerebral contusion N/A N/A No information
Extraocular motor nerve palsies N/A N/A No information
Chvostek's sign N/A N/A No information
Opisthotonos N/A N/A No information
Cryptococcal Meningitis approx 1 in 200,000 or 0.00% or 1,360 people in USA 1,360 about 5 per million
Leprosy approx 1 in 2,518,518 or 0.00% or 108 people in USA 108 108 annual cases notified in USA 1999 (MMWR 1999)
Glioblastoma N/A N/A No information
Myelopathy N/A N/A No information
Argyria N/A N/A No information
Piriformis Syndrome N/A N/A No information
Brudzinski's sign N/A N/A No information
Psoas sign N/A N/A No information
Footdrop N/A N/A No information
Renal-hepatic-pancreatic dysplasia -- Dandy Walker cyst N/A N/A No information
Oculopalatocerebral syndrome N/A N/A No information
Bone dysplasia -- corpus callosum agenesis N/A N/A No information
Olivopontocerebellar atrophy -- deafness N/A N/A No information
Microencephaly N/A N/A No information
Infantile onset spinocerebellar ataxia N/A N/A No information
Microcephaly nonsyndromal N/A N/A No information
Gliosarcoma N/A N/A No information
Juvenile-onset dystonia N/A N/A No information
Chorea familial benign N/A N/A No information
Post-traumatic epilepsy N/A N/A No information
Blepharoptosis N/A N/A No information
Bradykinesia N/A N/A No information
Bradyopsia N/A N/A No information
Brain Concussion N/A N/A No information
Epileptic encephalopathy, early infantile, 4 N/A N/A No information
Aneurysm, intracranial berry, 7 N/A N/A No information
Gangliosidosis GM1 type 3 N/A N/A No information
Primary amebic meningoencephalitis N/A N/A No information
Spinocerebellar ataxia, X-linked, 4 N/A N/A No information
GM1 gangliosidosis N/A N/A No information
Gangliosidosis, generalized GM1 type 2 N/A N/A No information
Gangliosidosis, generalized GM1 type 3 N/A N/A No information
Gangliosidosis generalized GM1, type 1 N/A N/A No information
Spinocerebellar ataxia, Machado-Joseph type IV N/A N/A No information
Spinocerebellar degenerescence, book type N/A N/A No information
Spinocerebellar ataxia, Machado-Joseph type III N/A N/A No information
Spinocerebellar ataxia 10 N/A N/A No information
Spinocerebellar ataxia, Machado-Joseph type II N/A N/A No information
Spinocerebellar ataxia, Machado-Joseph type V N/A N/A No information
Spinocerebellar ataxia -- amyotrophy -- deafness N/A N/A No information
Spinocerebellar ataxia-dysmorphism syndrome N/A N/A No information
Neuraminidase deficiency N/A N/A No information
Neuraminidase deficiency, type II, juvenile form N/A N/A No information
Cockayne syndrome N/A N/A No information
Cockayne syndrome type 1 N/A N/A No information
Cockayne syndrome type 2 N/A N/A No information
Cockayne syndrome type 3 N/A N/A No information
Galloway-Mowat Syndrome N/A N/A No information
Galloway syndrome N/A N/A No information
Nephrosis neuronal dysmigration Syndrome N/A N/A No information
SUNCT headache N/A N/A No information
Hallervorden-Spatz disease N/A N/A No information
Hallervorden-Spatz Syndrome N/A N/A No information
Porencephaly N/A N/A No information
Hydrocephalus approx 1 in 105,263 or 0.00% or 2,584 people in USA 2,584 6.46 per 10,000 births in the UK 2002 for hydrocephaly (University of Ulster, 2003)
Marinesco-Sjogren syndrome N/A N/A No information
Marinesco-Sjogren I N/A N/A No information
Chylomicron retention disease with Marinesco-Sjogren syndrome N/A N/A No information
Marinesco-Sjogren-like syndrome (MSLS) N/A N/A No information
Partial agenesis of corpus callosum N/A N/A No information
Partial lissencephaly N/A N/A No information
Neurofibromatosis-Noonan syndrome N/A N/A No information
Migraine with or without aura, susceptibility to, 4 N/A N/A No information
Dystonia-Parkinsonism, Adult-Onset N/A N/A No information
Migraine with or without aura, susceptibility to, 5 N/A N/A No information
Limbic encephalitis N/A N/A No information
Cataract-glaucoma N/A N/A No information
Opitc atrophy and cataract, autosomal dominant N/A N/A No information
Hemiplegic migraine, familial type 1 N/A N/A No information
Hemiplegic migraine, familial type 2 N/A N/A No information
Hemiplegic migraine, familial type 3 N/A N/A No information
Hemiplegic migraine, familial type 4 N/A N/A No information
Migraine with or without aura, susceptibility to, 1 N/A N/A No information
Migraine with or without aura, susceptibility to, 3 N/A N/A No information
Migraine with or without aura, susceptibility to, 6 N/A N/A No information
Migraine with or without aura, susceptibility to, 7 N/A N/A No information
Migraine with or without aura, susceptibility to, 8 N/A N/A No information
Hemiplegic migraine, familial N/A N/A No information
Torsion dystonia, autosomal recessive N/A N/A No information
Albinism ocular late onset sensorineural deafness N/A N/A No information
Microcephaly albinism digital anomalies syndrome N/A N/A No information
Chorioretinopathy dominant form -- microcephaly N/A N/A No information
Retinopathy pigmentary -- intellectual deficit N/A N/A No information
Proximal spinal muscular atrophy, type 4 N/A N/A No information
Proximal spinal muscular atrophy N/A N/A No information
Congenital benign spinal muscular atrophy dominant N/A N/A No information
Pontocerebellar hypoplasia with infantile spinal muscular atrophy N/A N/A No information
Arthrogryposis -- spinal muscular atrophy N/A N/A No information
Progressive spinal muscular atrophy N/A N/A No information
Spinal muscular atrophy -- Dandy-Walker complex -- cataracts N/A N/A No information
SPG N/A N/A No information
Spinal muscular atrophy, scapuloperoneal N/A N/A No information
Proximal spinal muscular atrophy, type 1 N/A N/A No information
Microcephaly -- lymphoedema -- chorioretinopathy N/A N/A No information
Microcephaly -- lymphoedema -- Chorioretinopathy Dysplasia Syndrome N/A N/A No information
MLCRD Syndrome N/A N/A No information
Lymphoedema -- Microcephaly -- Chorioretinopathy Syndrome N/A N/A No information
Lymphoedema -- Microcephaly -- chorioretinopathy N/A N/A No information
Corneal dystrophy -- perceptive deafness N/A N/A No information
Corneal anesthesia deafness intellectual deficit N/A N/A No information
Corneal hypesthesia deafness intellectual deficit N/A N/A No information
Corneal dystrophy and perceptive deafness N/A N/A No information
Corneal dystrophy -- ichthyosis -- microcephaly -- mental retardation N/A N/A No information
Rett-like syndrome N/A N/A No information
Dysphasic dementia, hereditary N/A N/A No information
Microcephaly, primary autosomal recessive, 1 N/A N/A No information
Microcephaly, primary autosomal recessive, 2 N/A N/A No information
Microcephaly, primary autosomal recessive, 4 N/A N/A No information
Microcephaly, primary autosomal recessive, 5 N/A N/A No information
Microcephaly, primary autosomal recessive, 6 N/A N/A No information
Microcephaly with normal intelligence, immunodeficiency N/A N/A No information
Neurogenic hypertension N/A N/A No information
Carnosinase deficiency N/A N/A No information
Olivopontocerebellar Atrophy, Hereditary N/A N/A No information
Olivopontocerebellar Atrophy N/A N/A No information
Olivopontocerebellar atrophy type IV N/A N/A No information
Olivopontocerebellar atrophy type 3 N/A N/A No information
Olivopontocerebellar atrophy I N/A N/A No information
Olivopontocerebellar atrophy, type V N/A N/A No information
Micrencephaly olivopontocerebellar hypoplasia N/A N/A No information
Benign familial infantile seizures 1 N/A N/A No information
Benign familial infantile seizures 2 N/A N/A No information
Retinal degeneration -- nanophthalmos -- glaucoma N/A N/A No information
Benign familial neonatal-infantile seizures N/A N/A No information
Seizures, benign familial neonatal-infantile N/A N/A No information
Auditory seizure N/A N/A No information
Photosensitive seizures N/A N/A No information
Somatosensory seizure N/A N/A No information
Epilepsy, pyridoxin-dependent N/A N/A No information
Epilepsy, Pyridoxine-Dependent N/A N/A No information
Classical pyridoxine-dependent seizures N/A N/A No information
Atypical pyridoxine-dependent seizures N/A N/A No information
Febrile Seizures N/A N/A No information
Kifafa seizure disorder N/A N/A No information
Epilepsy with myoclonic-astatic crisis N/A N/A No information
Epilepsy, benign occipital N/A N/A No information
Epilepsy, partial, familial N/A N/A No information
Epilepsy benign neonatal recessive form N/A N/A No information
Photosensitive epilepsy N/A N/A No information
Myokymia with neonatal epilepsy N/A N/A No information
Familial partial epilepsy with variable focus N/A N/A No information
Centrotemporal epilepsy N/A N/A No information
Infant epilepsy with migrant focal crisis N/A N/A No information
Epilepsy -- mental deterioration, Finnish type N/A N/A No information
Benign familial infantile epilepsy N/A N/A No information
Epilepsy occipital calcifications N/A N/A No information
Epilepsy juvenile absence N/A N/A No information
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp N/A N/A No information
Convulsions benign familial neonatal dominant form N/A N/A No information
Aphasia-epilepsy, acquired N/A N/A No information
Myoclonic epilepsy benign, adult, familial N/A N/A No information
Epilepsy with myoclonic absences N/A N/A No information
Epilepsy, generalized -- paroxysmal dyskinesia N/A N/A No information
Epilepsy, idiopathic generalized, susceptibility to N/A N/A No information
Epilepsy, benign familial neonatal N/A N/A No information
Epilepsy, familial mesial temporal lobe N/A N/A No information
Epilepsy, idiopathic generalized, susceptibility to, 1 N/A N/A No information
Epilepsy, idiopathic generalized, susceptibility to, 2 N/A N/A No information
Epilepsy, idiopathic generalized, susceptibility to, 3 N/A N/A No information
Epilepsy, idiopathic generalized, susceptibility to, 4 N/A N/A No information
Epilepsy, idiopathic generalized, susceptibility to, 5 N/A N/A No information
Epilepsy, idiopathic generalized, susceptibility to, 6 N/A N/A No information
Epilepsy, X-linked -- learning disabilities -- behavior disorders N/A N/A No information
Cortical dysplasia -- focal epilepsy syndrome N/A N/A No information
Epilepsy, familial temporal lobe, 4 N/A N/A No information
Generalized epilepsy and paroxysmal dyskinesia N/A N/A No information
Hemiconvulsion-Hemiplegia-Epilepsy syndrome N/A N/A No information
Epilepsy, nocturnal, frontal lobe type N/A N/A No information
Epilepsy, idiopathic generalized N/A N/A No information
Epilepsy, progressive myoclonic 3 N/A N/A No information
Epilepsy, nocturnal, frontal lobe type 1 N/A N/A No information
Epilepsy, nocturnal, frontal lobe type 2 N/A N/A No information
Epilepsy, nocturnal, frontal lobe type 3 N/A N/A No information
Epilepsy, nocturnal, frontal lobe type 4 N/A N/A No information
Hyperekplexia and epilepsy N/A N/A No information
Mediterranean myoclonic epilepsy N/A N/A No information
Baltic myoclonic epilepsy N/A N/A No information
Epilepsy, myoclonic progressive familial N/A N/A No information
Myoclonus with epilepsy with ragged red fibers N/A N/A No information
Juvenile myoclonic epilepsy N/A N/A No information
Infantile epileptic-dyskinetic encephalopathy N/A N/A No information
Myoclonus progressive epilepsy of Unverricht and Lundborg N/A N/A No information
Genetic reflex epilepsy N/A N/A No information
Epilepsy benign neonatal dominant form N/A N/A No information
Epilepsy -- microcephaly -- skeletal dysplasia N/A N/A No information
Infantile convulsions and paroxysmal choreoathetosis, familial N/A N/A No information
Convulsions, benign familial infantile, 1 N/A N/A No information
Focal dystonia N/A N/A No information
Neuronopathy, distal hereditary motor, type IV N/A N/A No information
Dystonia 15, myoclonic N/A N/A No information
California encephalitis N/A N/A No information
Myotonic dystrophy type 3 N/A N/A No information
Congenital myotonic dystrophy N/A N/A No information
Myotonic dystrophy, type 2 N/A N/A No information
Proximal myotonic dystrophy N/A N/A No information
Cerebellar degeneration N/A N/A No information
Dystonia 4, Torsion, Autosomal Dominant N/A N/A No information
Cerebral sarcoma N/A N/A No information
Choreoathetosis-spasticity, episodic N/A N/A No information
Transthyretin amyloidosis N/A N/A No information
Amyloidosis, cerebroarterial, hereditary, Italian type N/A N/A No information
Amyloidosis VII N/A N/A No information
Amyloidosis, oculoleptomeningeal N/A N/A No information
Amyloidosis, cerebroarterial, hereditary, Iowa type N/A N/A No information
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type N/A N/A No information
Arthrogryposis multiplex congenita neurogenic type N/A N/A No information
Central nervous system lymphoma, primary N/A N/A No information
Motor neuropathy, peripheral with dysautonomia N/A N/A No information
Sensory neuropathy type 1 N/A N/A No information
Neuropathy hereditary sensory and autonomic type 1 N/A N/A No information
Neuropathy -- ataxia -- retinitis pigmentosa N/A N/A No information
Motor and Sensory Neuropathy, Optic Atrophy and Sensorineural Hearing Loss N/A N/A No information
Motor and Sensory Neuropathy with Sensorineural Hearing Loss, Bouldin type N/A N/A No information
Hereditary Motor and Sensory Neuropathy with Deafness, Mental Retardation and Absence of Large Myelinated Fibers N/A N/A No information
Motor and Sensory Neuropathy, Pigmentary Retinopathy and Sensorineural Hearing Loss N/A N/A No information
Hypomyelination neuropathy -- arthrogryposis N/A N/A No information
Lissencephaly, type 1, isolated, without known genetic defects N/A N/A No information
Neuropathy congenital sensory neurotrophic keratitis N/A N/A No information
Neuropathy hereditary with liability to pressure palsies N/A N/A No information
Multifocal motor neuropathy with conduction block N/A N/A No information
Hereditary sensory and autonomic neuropathy 3 N/A N/A No information
Hereditary sensory neuropathy type 1 N/A N/A No information
Hereditary sensory neuropathy type 2 N/A N/A No information
Neuropathy ataxia and retinis pigmentosa N/A N/A No information
Hereditary neuropathy with liability to pressure palsies N/A N/A No information
Moebius axonal neuropathy -- hypogonadism N/A N/A No information
Polyneuropathy -- hand defect N/A N/A No information
Polyneuropathy N/A N/A No information
Osteopetrosis with neuroaxonal dysplasia, infantile form N/A N/A No information
Lissencephaly type III -- metacarpal bone dysplasia N/A N/A No information
Niemann-Pick disease N/A N/A No information
Niemann-Pick disease, type A N/A N/A No information
Niemann-Pick disease, type D N/A N/A No information
Niemann-Pick disease, type C1 N/A N/A No information
Niemann-Pick disease, type C2 N/A N/A No information
Niemann-Pick disease, type B N/A N/A No information
Cervical hypertrichosis neuropathy N/A N/A No information
Pena Shokeir syndrome, type 1 N/A N/A No information
Pena-Shokeir syndrome Type 2 N/A N/A No information
COFS syndrome N/A N/A No information
Cerebro-Oculo-Facio-Skeletal Syndrome N/A N/A No information
Tolosa-Hunt Syndrome N/A N/A No information
Neuropathy, hereditary motor and sensory, LOM type N/A N/A No information
Neuropathy, hereditary motor and sensory, Okinawa type N/A N/A No information
Dejerine-Sottas Syndrome N/A N/A No information
Hypertrophic neuropathy of Dejerine-Sottas N/A N/A No information
Dejerine-Sottas disease N/A N/A No information
Wieacker-Wolff Syndrome N/A N/A No information
Lissencephaly syndrome type 1 N/A N/A No information
Demyelinating disorder N/A N/A No information
Microcephaly, primary autosomal recessive, 7 N/A N/A No information
Developmental delay -- epilepsy -- neonatal diabetes N/A N/A No information
Corpus callosum agenesis double urinary collecting system and trigonocephaly N/A N/A No information
Corpus callosum agenesis double urinary collecting N/A N/A No information
Deafness mesenteric diverticula of small bowel neuropathy N/A N/A No information
Atherosclerosis- deafness -- diabetes -- epilepsy -- nephropathy N/A N/A No information
Atherosclerosis, premature -- deafness -- diabetes mellitus -- photomyoclonus -- nephropathy -- degenerative neurologic disease N/A N/A No information
Spastic paraplegia nephritis deafness N/A N/A No information
Diabetes, neonatal -- congenital hypothyroidism -- congenital glaucoma -- hepatic fibrosis -- polycystic kidneys N/A N/A No information
Renal tubulopathy -- diabetes mellitus -- cerebellar ataxia N/A N/A No information
Lissencephaly, type 1, X-linked N/A N/A No information
Ataxia Telangiectasia N/A N/A No information
Encephalophathy recurrent of childhood N/A N/A No information
Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss N/A N/A No information
Auditory neuropathy N/A N/A No information
Primary lateral sclerosis, adult N/A N/A No information
Arthropathy, Neurogenic N/A N/A No information
Neuronopathy, distal, autosomal recessive, 3 N/A N/A No information
Episodic ataxia syndrome N/A N/A No information
Episodic kinesigenic dyskinesia 2 N/A N/A No information
Dystonia with cerebellar atrophy N/A N/A No information
Lissencephaly type III -- familial foetal akinesia sequence N/A N/A No information
Lissencephaly, X linked -- agenesis of the corpus callosum -- genital anomalies N/A N/A No information
Lissencephaly -- immunodeficiency N/A N/A No information
Lissencephaly, isolated N/A N/A No information
Lissencephaly with cerebellar hypoplasia N/A N/A No information
Lissencephaly, X-linked, 1 N/A N/A No information
Lissencephaly with cerebellar hypoplasia, recessive N/A N/A No information
Lissencephaly type 2 N/A N/A No information
Lissencephaly, X-linked 2 N/A N/A No information
Lissencephaly type 1, due to LIS 1 anomalies N/A N/A No information
Cerebellar degeneration, subacute N/A N/A No information
Lennox-Gastaut Syndrome N/A N/A No information
Hypomelanosis of Ito N/A N/A No information
Ichthyosis mental retardation asymptomatic spasticity N/A N/A No information
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome N/A N/A No information
Congenital ichthyosis, microcephalus, quadriplegia N/A N/A No information
Hydrocephalus -- costovertebral dysplasia -- Sprengel anomaly N/A N/A No information
Arthrogrypotic hand abnormality and sensorineural hearing loss N/A N/A No information
Arthrogryposis -- epileptic seizures -- migrational brain disorder N/A N/A No information
Arthrogryposis-like hand anomaly -- sensorineural deafness N/A N/A No information
Dystonia 12 N/A N/A No information
Dystonia musculorum deforms 4 N/A N/A No information
Dystonia 13, torsion N/A N/A No information
Dystonia 14 N/A N/A No information
Dystonia 3, torsion, X-linked N/A N/A No information
Dystonia 7, torsion N/A N/A No information
Dystonia 1, Torsion, Autosomal Dominant N/A N/A No information
Dystonia Musculorum Deformans 1 N/A N/A No information
Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency N/A N/A No information
Borjeson-Forssman-Lehmann Syndrome N/A N/A No information
Optic atrophy N/A N/A No information
Optic atrophy -- ophthalmoplegia -- ptosis -- deafness -- myopathy N/A N/A No information
Optic atrophy, hearing loss and peripheral neuropathy N/A N/A No information
Optic atrophy, deafness and peripheral neuropathy N/A N/A No information
Optic atrophy, hearing loss and peripheral neuropathy, autosomal recessive N/A N/A No information
Optic atrophy deafness neuropathy N/A N/A No information
Optic Atrophy -- Hearing Loss -- Peripheral Neuropathy, Autosomal Dominant N/A N/A No information
Optic atrophy opthalmoplegia ptosis deafness myopia N/A N/A No information
Hydrocephaly tall stature joint laxity N/A N/A No information
Hydrocephaly tall stature joint laxity and kyphoscoliosis N/A N/A No information
Deafness, Conductive Stapedial, With Ear Malformation and Facial Palsy N/A N/A No information
Microcephaly syndactyly brachymesophalangy N/A N/A No information
Progressive neurodegeneration -- joint laxity -- cataract N/A N/A No information
Microcephaly developmental delay pancytopenia N/A N/A No information
Intellectual deficit -- cataracts -- calcified pinnae -- myopathy N/A N/A No information
Ataxia -- hypogonadism -- choroidal dystrophy N/A N/A No information
Neurofibrosarcoma N/A N/A No information
Herpes simplex encephalitis N/A N/A No information
Autoimmune peripheral neuropathy N/A N/A No information
Cerebro-facio-thoracic dysplasia N/A N/A No information
Cerebral abscess N/A N/A No information
Cerebellar abscess N/A N/A No information
Malignant Buotonneuse fever N/A N/A No information
Rhino-orbito-cerebral phycomycosis N/A N/A No information
Rocio encephalitis N/A N/A No information
Venezuelan equine encephalitis N/A N/A No information
Absence of septum pellucidum with porencephalia syndrome N/A N/A No information
Achalasia -- adrenal -- alacrima syndrome N/A N/A No information
Acrodynia N/A N/A No information
Addington disease N/A N/A No information
Aging brain syndrome N/A N/A No information
Polio approx 1 in 0 or 0.00% or 0 people in USA 0 0 annual cases of paralytic poliomyelitis notified in USA 1999 (MMWR 1999)
Rabies approx 1 in 15,111 or 0.01% or 18,000 people in USA 18,000 18,000 cases (of rabies shots rather than actual rabies)
Viral meningitis approx 1 in 30,452 or 0.00% or 8,932 people in USA 8,932 8,932 new cases in America 1995 (Meningitis Foundation of America, CDC, 1994)
Rosenberg-Chutorian Syndrome N/A N/A No information
Stargardt Macular Degeneration, Absent or Hypoplastic Corpus Callosum, Mental Retardation and Dysmorphic Features N/A N/A No information
Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance N/A N/A No information
Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance N/A N/A No information
Hypotonia, Seizures and Precocious Puberty N/A N/A No information
Bickerstaff's brainstem encephalitis N/A N/A No information
Cerebral malaria N/A N/A No information
Neurocysticercosis N/A N/A No information
Horner's syndrome N/A N/A No information
Sjogren-Larsson syndrome N/A N/A No information
Cephalic tetanus N/A N/A No information
Meningococcal disease approx 1 in 108,756 or 0.00% or 2,500 people in USA 2,500 2,501 annual cases notified in USA 1999 (MMWR 1999)
Myelitis N/A N/A No information
Encephalomyelitis N/A N/A No information
Spina bifida approx 1 in 1,133,333 or 0.00% or 240 people in USA 240 6 per 100,000 births
Congenital SMA with arthrogryposis N/A N/A No information
Meningomyelocele N/A N/A No information
Renal agenesis -- meningomyelocele -- mullerian defect N/A N/A No information
Anencephaly and spina bifida X-linked N/A N/A No information
Lipomyelomeningocele N/A N/A No information
Meningocele N/A N/A No information
Sacral meningocele -- conotruncal heart defects N/A N/A No information
Sacral defect and anterior sacral meningocele N/A N/A No information
Lateral meningocele syndrome N/A N/A No information
Perineal hemangioma -- external genitalia malformations -- lipomyelomeningocele -- vesicorenal abnormalities -- imperforate anus N/A N/A No information
Flaccid dysarthria N/A N/A No information
Corpus callosum dysgenesis X-linked recessive N/A N/A No information
Ectodermal dysplasia -- hypohidrotic -- hypothyroidism -- ciliary dyskinesia N/A N/A No information
Friedreich ataxia -- congenital glaucoma N/A N/A No information
Ophthalmoplegia N/A N/A No information
Transmissible mink encephalopathy N/A N/A No information
Calcification of basal ganglia with or without hypocalcemia N/A N/A No information
Dialysis encephalopathy syndrome N/A N/A No information
Hepatic encephalopathy syndrome N/A N/A No information
Tuberculous meningitis N/A N/A No information
Malformations in neuronal migration N/A N/A No information
Spongiform encephalopathy N/A N/A No information
Cerebral cavernous malformations N/A N/A No information
Vacuolar myopathy N/A N/A No information
Hereditary inclusion body myopathy -- joint contractures -- ophthalmoplegia N/A N/A No information
Glycine encephalopathy, atypical mild form N/A N/A No information
Glycine encephalopathy, classical neonatal early-onset form N/A N/A No information
Glycine encephalopathy, transient neontal form N/A N/A No information
Scapuloperoneal amyotrophy N/A N/A No information
Glycine encephalopathy, classical neonatal form N/A N/A No information
Glycine encephalopathy, classical neonatal late-onset form N/A N/A No information
Amyotrophy, neurogenic scapuloperoneal, New England type N/A N/A No information
Scapuloperoneal syndrome, neurogenic, Kaeser type N/A N/A No information
Scapuloperoneal myopathy, MYH7-related N/A N/A No information
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia N/A N/A No information
Cardioencephalomyopathy fatal infantile due to cytochrome c oxidase deficiency N/A N/A No information
Brody myopathy N/A N/A No information
Myopathy -- ophthalmoplegia -- hypoacousia -- areflexia N/A N/A No information
Mitochondrial encephalomyopathy -- aminoacidopathy N/A N/A No information
Muscular dystrophy -- white matter spongiosis N/A N/A No information
Scleroatonic muscular dystrophy N/A N/A No information
Hypotonic sclerotic muscular dystrophy N/A N/A No information
Congenital muscular dystrophy syringomyelia N/A N/A No information
Facioscapulohumeral Muscular Dystrophy -- Sensorineural Hearing Loss N/A N/A No information
Syringomyelia N/A N/A No information
Tethered Spinal Cord Syndrome N/A N/A No information
Syringomyelia, cervical lesion N/A N/A No information
Syringomyelia, medulla oblongata lesion N/A N/A No information
Syringomyelia, lumbar lesion N/A N/A No information
Variant Creutzfeldt-Jakob disease N/A N/A No information
Prion disease approx 1 in 906,666 or 0.00% or 300 people in USA 299 approximately 300 cases of prion disease are diagnosed in the US each year, Genetics Home Reference website
Hydrocephaly corpus callosum agenesis diaphragmatic hernia N/A N/A No information
Nasopharyngeal teratoma with Dandy-Walker -- diaphragmatic hernia N/A N/A No information
Diaphragmatic hernia -- exomphalos -- corpus callosum agenesis N/A N/A No information
Primary orthostatic tremor N/A N/A No information
Holoprosencephaly deletion 2p N/A N/A No information
Post-Streptococcal Neurologic Disorders N/A N/A No information
Neurotoxicity syndromes N/A N/A No information
Meningoencephalocele -- arthrogryposis -- hypoplastic thumb N/A N/A No information
Tick-borne encephalitis N/A N/A No information
Renal tubular acidosis progressive nerve deafness N/A N/A No information
Neuroaxonal dystrophy -- renal tubular acidosis N/A N/A No information
Schwannoma, malignant N/A N/A No information
Spinal cord neoplasm N/A N/A No information
Ceroid storage disease N/A N/A No information
Decreased cerebral perfusion N/A N/A No information
Decreased ankle and knee reflexes N/A N/A No information
Decorticate posture N/A N/A No information
Decorticate posture in children N/A N/A No information
Nephronophthisis familial, adult -- spastic quadriparesis N/A N/A No information
Tremor hereditary essential, 1 N/A N/A No information
Tremor hereditary essential, 2 N/A N/A No information
Tremor, hereditary essential, and idiopathic normal pressure hydrocpehalus N/A N/A No information
Tremor, hereditary essential, and idiopathic normal pressure hydrocephalus N/A N/A No information
Alopecia, mental retardation and neurological problems N/A N/A No information
Pontoneocerebellar Hypoplasia N/A N/A No information
Neurosarcoidosis N/A N/A No information
Microcephaly -- mental retardation -- spasticity -- epilepsy N/A N/A No information
Pellagra-like syndrome N/A N/A No information
Franek-Bocker-Kahlen syndrome N/A N/A No information
Microcephaly brain defect spasticity hypernatremia N/A N/A No information
Torsion dystonia with onset in infancy N/A N/A No information
Oculocerebral dysplasia N/A N/A No information
Spasticity -- multiple exostoses N/A N/A No information
$2-methylglutaconic aciduria type 3$ N/A N/A No information
Colorado tick encephalitis N/A N/A No information
Bickerstaff's brainstem encephalitis (BBE) N/A N/A No information
Hirschsprung disease ganglioneuroblastoma N/A N/A No information
Zellweger Syndrome N/A N/A No information
Lathyrism N/A N/A No information
Von Hippel-Lindau Disease N/A N/A No information
Angelman syndrome N/A N/A No information
Progressive External Opthhalmoplegia, Autosomal Dominant, 5 N/A N/A No information
Progressive External Opthhalmoplegia, Autosomal Dominant, 4 N/A N/A No information
Progressive External Opthhalmoplegia, Autosomal Dominant, 3 N/A N/A No information
Progressive External Opthhalmoplegia, Autosomal Dominant, 2 N/A N/A No information
Progressive External Opthhalmoplegia, Autosomal Dominant, 1 N/A N/A No information
Progressive External Opthhalmoplegia, Autosomal Dominant N/A N/A No information
Hypothalamic dysfunction N/A N/A No information
Hypothalamic hamartomas N/A N/A No information
Symmetrical thalamic calcifications N/A N/A No information
Thalamic degeneration symmetrical infantile N/A N/A No information
Infantile striato-thalamic degeneration N/A N/A No information
Thalamic degenerescence infantile N/A N/A No information
Dejerine-Roussy syndrome N/A N/A No information
Roussy-Levy hereditary areflexic dystasia N/A N/A No information
Granulomatous amoebic encephalitis N/A N/A No information
Andrade's syndrome N/A N/A No information
Akinetic mutism N/A N/A No information
Neuropathy, distal hereditary motor, Jerash type N/A N/A No information
Neurodegeneration due to Cerebral Folate Transport Deficiency N/A N/A No information
Thoracic dysplasia -- hydrocephalus syndrome N/A N/A No information
Brachydactyly nystagmus cerebellar ataxia N/A N/A No information
Agyria pachygyria polymicrogyria N/A N/A No information
Hydrocephalus obesity hypogonadism N/A N/A No information
Microcephaly immunodeficiency lymphoreticuloma N/A N/A No information
Microcephaly, hiatal hernia and nephrotic syndrome N/A N/A No information
Gerstmann Syndrome N/A N/A No information
Partington X-linked mental retardation syndrome N/A N/A No information
Progressive supranuclear palsy, atypical N/A N/A No information
Syncope, familial neurocardiogenic N/A N/A No information
Nerve sheath neoplasm N/A N/A No information
Spastic tetraplegic -- cerebral palsy N/A N/A No information
Microcephaly with chorioretinopathy, autosomal dominant form N/A N/A No information
Precocious myoclonic encephalopathy N/A N/A No information
Primary progressive aphasia N/A N/A No information
Neurofibromatosis, familial intestinal N/A N/A No information
Hypoplastic right heart -- microcephaly N/A N/A No information
Spasticity -- mental retardation N/A N/A No information
Microcephaly -- pontocerebellar hypoplasia -- dyskinesia N/A N/A No information
Motor neuropathy N/A N/A No information
Hydrocephalus autosomal recessive N/A N/A No information
Cerebral palsy, spastic, diplegic N/A N/A No information
Brain Stem Neoplasms N/A N/A No information
Dandy Walker syndrome recessive form N/A N/A No information
Chorea, remitting with nystagmus and cataracts N/A N/A No information
Ovarioleukodystrophy N/A N/A No information
Acute hemorrhagic leukoencephalitis N/A N/A No information
Familial neurocardiogenic syncope N/A N/A No information
Cerebral ventricle neoplasm N/A N/A No information
Patau syndrome approx 1 in 5,000 or 0.02% or 54,400 people in USA 54,399 1-in-5000 approximately.
Chediak-Higashi Syndrome N/A N/A No information
Tay-Sachs disease -- adult onset N/A N/A No information
Tay Sachs N/A N/A No information
Tay Sachs Disease N/A N/A No information
Huntington's Disease approx 1 in 175,390 or 0.00% or 1,550 people in USA 1,550 26 annual cases in Victoria 1996 (DHS-VIC)
Machado-Joseph Disease N/A N/A No information
Dentatorubral Pallidoluysian Atrophy N/A N/A No information
MELAS N/A N/A No information
Rett's syndrome approx 1 in 10,000 or 0.01% or 27,200 people in USA 27,199 1 in 10,000-15,000 live female births
Lafora body disease N/A N/A No information
Alexander Syndrome N/A N/A No information
Binswanger's Disease N/A N/A No information
Brachial Plexus Injury N/A N/A No information
Brown-Sequard Syndrome N/A N/A No information
Canavan disease N/A N/A No information
Chronic Inflammatory Demyelinating Polyneuropathy N/A N/A No information
Erb's Palsy N/A N/A No information
Allergic encephalomyelitis N/A N/A No information
Epileptic encephalopathy, early infantile, 3 N/A N/A No information
Epileptic encephalopathy, early infantile, 1 N/A N/A No information
Epileptic encephalopathy, early infantile, 2 N/A N/A No information
Aneurysm, intracranial berry, 8 N/A N/A No information
Anotia -- facial palsy -- cardiac defect N/A N/A No information
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response N/A N/A No information
HHV-6 encephalitis N/A N/A No information
Dementia, familial Danish N/A N/A No information
Cerebellar ataxia, infantile with progressive external ophthalmoplegia N/A N/A No information
Celiac disease -- epilepsy -- occipital calcifications N/A N/A No information
Presenile dementia, Kraepelin type N/A N/A No information
Spasticity -- mental retardation -- epilepsy, X-linked N/A N/A No information
Spastic paraplegia glaucoma precocious puberty N/A N/A No information
Leukoencephalopathy, arthritis, colitis and hypogammaglobulinemia N/A N/A No information
Cerebrotendinous Xanthomatosus N/A N/A No information
Leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema N/A N/A No information
Microcephaly approx 1 in 666,666 or 0.00% or 407 people in USA 407 1.02 per 10,000 births in the UK 2002 for microcephaly (University of Ulster, 2003)
Tay-Sachs disease -- juvenile onset N/A N/A No information
Vascular malformations of the brain N/A N/A No information
Torsion dystonia N/A N/A No information
Juvenile primary lateral sclerosis N/A N/A No information
Krabbe disease, atypical, due to saposin A deficiency N/A N/A No information
Familial infantile metachromatic leukodystrophy -- late infantile N/A N/A No information
Refsum disease with increased pipecolic acidemia N/A N/A No information
Infantile Refsum Disease N/A N/A No information
Folinic acid-responsive seizures N/A N/A No information
ARCA N/A N/A No information
Fetal akinesia syndrome, X-linked N/A N/A No information
Focal cortical dysplasia N/A N/A No information
Focal cortical dysplasia type II N/A N/A No information
Focal cortical dysplasia type IIA N/A N/A No information
Focal cortical dysplasia type IIB N/A N/A No information
Non-lissencephalic cortical dysplasia N/A N/A No information
Krabbe leukodystrophy N/A N/A No information
Metachromatic Leukodystrophy N/A N/A No information
Renal Cell Carcinoma Associated with Neuroblastoma N/A N/A No information
Agammaglobulinemia, microcephaly, and severe dermatitis N/A N/A No information
Hypobetalipoproteinaemia -- ataxia -- hearing loss N/A N/A No information
Encephalopathy due to sulphite oxidase deficiency N/A N/A No information
Auditory Processing Disorder N/A N/A No information
Dandy-Walker malformation with mental retardation, basal ganglia disease, and seizures N/A N/A No information
Neuroaxonal dystrophy, infantile N/A N/A No information
Neurodegenerative syndrome, X-linked, Bertini type N/A N/A No information
Neurodegenerative syndrome, X-linked, Hamel type N/A N/A No information
Visceral neuropathy -- brain anomalies -- facial dysmorphism -- developmental delay N/A N/A No information
Agnathia-holoprosencephaly-situs inversus N/A N/A No information
Wernicke dementia N/A N/A No information
Bone marrow failure -- neurologic abnormalities N/A N/A No information
Auditory perceptual disorder N/A N/A No information
Idiopathic basal ganglia calcification, childhood onset N/A N/A No information
Acoustic Neurinoma N/A N/A No information
Progressive cerebellocerebral atrophy N/A N/A No information
Infantile cerebellar atrophy N/A N/A No information
Herpes, Neonatal -- Central Nervous System Infection N/A N/A No information
Hereditary methemoglobinemia, recessive, type II N/A N/A No information
Acanthamoeba infection of the central nervous system N/A N/A No information
Simian B virus infection N/A N/A No information
Meningococcal infection N/A N/A No information
Sensorineural hearing loss N/A N/A No information
Rhinocerebral zygomycosis N/A N/A No information
Serratia cerebral abscess N/A N/A No information
Rhinocerebral mucormycosis N/A N/A No information
Rubella panencephalitis N/A N/A No information
Progressive Rubella Panencephalitis N/A N/A No information
Acute idiopathic polyneuritis N/A N/A No information
West nile encephalitis N/A N/A No information
FG syndrome 1 N/A N/A No information
FG syndrome 2 N/A N/A No information
FG syndrome 3 N/A N/A No information
FG syndrome 4 N/A N/A No information
FG syndrome 5 N/A N/A No information
Pseudotumor Cerebri N/A N/A No information
Neuroectodermal tumor, primitive N/A N/A No information
Neuroectodermal tumors primitive N/A N/A No information
Neural crest-derived tumors N/A N/A No information
Melanoma -- astrocytoma syndrome N/A N/A No information
Radiation induced meningioma N/A N/A No information
Cerebral astrocytoma, adult N/A N/A No information
Cerebellar ataxia, autosomal recessive N/A N/A No information
Cerebellar ataxia type 1, autosomal recessive N/A N/A No information
Cerebellar ataxia, X-linked N/A N/A No information
Cerebellar ataxia, dominant pure N/A N/A No information
Cerebellar agenesis N/A N/A No information
Cerebellar atrophy with progressive microcephaly N/A N/A No information
Central nervous system oxygen toxicity N/A N/A No information
Gastro-enteropancreatic neuroendocrine tumor N/A N/A No information
Neuroendocrine carcinoma of the cervix N/A N/A No information
Glioma N/A N/A No information
Desmoplastic cerebral astrocytoma of infancy N/A N/A No information
Neuroma biliary tract N/A N/A No information
Agammaglobulinemia -- microcephaly -- craniosynostosis -- severe dermatitis N/A N/A No information
Western/Eastern/California encephalitis N/A N/A No information
Sixth nerve palsy, benign N/A N/A No information
Refsum disease, infantile form N/A N/A No information
Nipah virus encephalitis N/A N/A No information
Autoimmune Diseases of the Nervous System N/A N/A No information
Hypomyelination and congenital cataract N/A N/A No information
Neurosyphilis N/A N/A No information
Benign essential tremor syndrome N/A N/A No information
Dyskinesia, paroxysmal N/A N/A No information
Myelinopathies N/A N/A No information
Paraneoplastic limbic encephalitis N/A N/A No information
Ependymoma N/A N/A No information
Aceruloplasminemia N/A N/A No information
Pineoblastoma, adult N/A N/A No information
Neuroacanthocytosis N/A N/A No information
Phenylketonuria type 2 N/A N/A No information
Hydroxykynureninuria N/A N/A No information
Methylmalonic aciduria -- microcephaly -- cataract N/A N/A No information
Optic pathway glioma N/A N/A No information
Seizures -- intellectual deficit due to hydroxylysinuria N/A N/A No information
Ganglioglioma N/A N/A No information
Gliomatosis cerebri N/A N/A No information
Desmoplastic infantile ganglioma N/A N/A No information
Benign astrocytoma N/A N/A No information
Malignant astrocytoma N/A N/A No information
Juvenile pilocytic astrocytoma N/A N/A No information
Adult low grade infiltrative supratentorial Astrocytoma N/A N/A No information
Childhood-onset cerebral X-linked adrenoleukodystrophy N/A N/A No information
Porphyria, hereditary coproporphyria N/A N/A No information
Cerebellar hypoplasia N/A N/A No information
Cerebellar ataxia -- ectodermal dysplasia N/A N/A No information
Cerebellar ataxia -- areflexia -- pes cavus -- optic atrophy -- sensorineural hearing loss N/A N/A No information
Cerebellar ataxia -- intellectual deficit -- optic atrophy -- skin abnormalities N/A N/A No information
Cerebellar Ataxia, Deafness and Narcolepsy N/A N/A No information
Cerebellar ataxia syndrome N/A N/A No information
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss N/A N/A No information
Cerebellar hypoplasia -- endosteal sclerosis N/A N/A No information
Cerebellar parenchymal degeneration N/A N/A No information
Dementia, familial British N/A N/A No information
Cerebellar hypoplasia -- tapetoretinal degeneration N/A N/A No information
Hereditary non-progressive cerebellar ataxia syndrome of early onset N/A N/A No information
Early-onset non-progressive cerebellar ataxia syndrome, dominantly inherited N/A N/A No information
Hereditary cerebellar ataxia syndrome of early onset N/A N/A No information
Cerebellar vermis hypoplasia -- oligophrenia -- congenital ataxia -- coloboma -- hepatic fibrosis N/A N/A No information
Cerebral calcification cerebellar hypoplasia N/A N/A No information
Anemia, sideroblastic spinocerebellar ataxia N/A N/A No information
Myelocerebellar disorder N/A N/A No information
Myoclonus, cerebellar ataxia, deafness N/A N/A No information
Coloboma chorioretinal cerebellar vermis aplasia N/A N/A No information
Prosencephaly -- cerebellar dysgenesis N/A N/A No information
Porencephaly -- cerebellar hypoplasia -- malformations N/A N/A No information
X-linked adrenoleukodystrophy -- Addison disease only approx 1 in 20 or 5.00% or 13.6 million people in USA 13,600,000 10% of males with X-linked adrenoleukodystrophy have the Addison only form of the disease, Genetics Home Reference website
Adrenoleukodystrophy, autosomal, neonatal form N/A N/A No information
Papillitis N/A N/A No information
Canavan leukodystrophy N/A N/A No information
Leukodystrophy with oligodontia N/A N/A No information
Pseudoadrenoleukodystrophy N/A N/A No information
Dermatoleukodystrophy N/A N/A No information
Vanishing white matter leukodystrophy N/A N/A No information
Medial Medullary Syndrome N/A N/A No information
Congenital stenosis of cervical medullary canal N/A N/A No information
Rokitansky Van Bogaert syndrome N/A N/A No information
Nyssen-Van Bogaert syndrome N/A N/A No information
Nyssen-Van Bogaert-Meyer syndrome N/A N/A No information
Adie syndrome N/A N/A No information
Primary glaucoma, congenital N/A N/A No information
Superficial siderosis of the central nervous system N/A N/A No information
Coloboma porencephaly hydronephrosis N/A N/A No information
Optic nerve coloboma with renal disease N/A N/A No information
Ectodermal dysplasia -- mental retardation -- central nervous system malformation N/A N/A No information
Developmental malformations -- deafness -- dystonia N/A N/A No information
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 N/A N/A No information
Median cleft, corpus callosum, lipoma, and cutaneous polyps N/A N/A No information
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa and Cataract N/A N/A No information
Endocrine-Cerebroosteodysplasia N/A N/A No information
Cystic leukoencephalopathy without megalencephaly N/A N/A No information
East Syndrome N/A N/A No information
Neurodegeneration With Brain Iron Accumulation 2 N/A N/A No information
Oppenheim's dystonia N/A N/A No information
Microcephaly-Faciocardioskeletal syndrome N/A N/A No information
Disseminated Sclerosis with Narcolepsy N/A N/A No information
Frontotemporal dementia N/A N/A No information
NOMID syndrome N/A N/A No information
Amelo-cerebro-hypohidrotic syndrome N/A N/A No information
Mitochondrial neurogastrointestinal encephalopathy syndrome N/A N/A No information
Chondrodysplasia -- disorder of sex development N/A N/A No information
Hydrocephalus -- Skeletal Anomalies -- Mental Disturbance N/A N/A No information
Hydrocephalus skeletal anomalies N/A N/A No information
Morning Glory Fundus Anomaly -- Optic Nerve Coloboma -- Porencephaly -- Hydronephrosis N/A N/A No information
Hereditary paroxysmal cerebral ataxia N/A N/A No information
Dysautonomia like disorder N/A N/A No information
Myasthenia, familial N/A N/A No information
Spinal AVM N/A N/A No information
Congenital brain dysgenesis due to glutamine synthetase deficiency N/A N/A No information
Idiopathic dystonia DYT1 N/A N/A No information
Neuroepithelioma N/A N/A No information
Unverricht-Lundborg disease N/A N/A No information
Unverricht-Lundborg syndrome N/A N/A No information
Schimmelpenning-Feurstein-Mims Syndrome N/A N/A No information
Microcephaly -- facial clefting -- preaxial polydactyly N/A N/A No information
Subependymoma N/A N/A No information
Anterior horn disease N/A N/A No information
Cerebral calcifications opalescent teeth phosphaturia N/A N/A No information
Morel-Wildi syndrome N/A N/A No information
Cerebelloolivary atrophy N/A N/A No information
Prosopagnosia, congenital N/A N/A No information
Mitochondrial DNA depletion syndrome N/A N/A No information
Corpus callosum dysgenesis cleft spasm N/A N/A No information
Thrombocytopenia -- Multiple Congenital Anomalies N/A N/A No information
Cataract -- Hypertrichosis -- Intellectual Deficit N/A N/A No information
Arena synddrome N/A N/A No information
Alcock syndrome N/A N/A No information
Ataxia, episodic -- vertigo -- tinnitus -- myokymia N/A N/A No information
Encephalopathy due to GLUT1 deficiency N/A N/A No information
Scapuloperoneal syndrome, neurogenic type N/A N/A No information
Neuropathy, Hereditary Sensory, Type IV N/A N/A No information
Neuropathy, hereditary, sensory, radicular N/A N/A No information
Norman-Roberts lissencephaly syndrome N/A N/A No information
HARD syndrome (Hydrocephalus -- agyria -- retinal dysplasia) N/A N/A No information
Paraplegia -- brachydactyly -- cone-shaped epiphysis N/A N/A No information
Marek disease N/A N/A No information
Marek's disease N/A N/A No information
Fowl Paralysis N/A N/A No information
Fowl paralyses N/A N/A No information
Mareck's disease -- nervous system N/A N/A No information
Wolfram's disease N/A N/A No information
Neurofibromatosis-2 N/A N/A No information
Neurofibromatosis approx 1 in 3,000 or 0.03% or 90,666 people in USA 90,666 about 1 in 30001.
Vestibular neuronitis N/A N/A No information
Segmental neurofibromatosis N/A N/A No information
Microcephaly, primary autosomal recessive N/A N/A No information
Peripheral type neurofibromatosis N/A N/A No information
Pheochromocytoma as part of Neurofibromatosis N/A N/A No information
Neurofibromatosis, type 4, of Riccardi N/A N/A No information
Neurofibromatosis type 3A N/A N/A No information
Neurofibromatosis type 3B N/A N/A No information
Neurofibromatosis type 6 N/A N/A No information
Neurofibromatosis Type 1 (NF-1) N/A N/A No information
Neurofibromatosis-1 N/A N/A No information
Neurofibromatosis syndrome Type II N/A N/A No information
Neurofibromatosis syndrome N/A N/A No information
Neuropathy, congenital, with arthrogryposis multiplex N/A N/A No information
Peroxisomal Biogenesis Disorders N/A N/A No information
Peroxisome biogenesis disorders N/A N/A No information
Peroxisomal defects N/A N/A No information
Liver disease -- retinitis pigmentosa -- polyneuropathy -- epilepsy N/A N/A No information
Heterotopia, periventricular, associated with chromosome 5p anomalies N/A N/A No information
Griscelli disease N/A N/A No information
Griscelli syndrome type I N/A N/A No information
Griscelli syndrome type II N/A N/A No information
Papilledema N/A N/A No information
Brain malformation -- congenital heart disease -- postaxial polydactyly N/A N/A No information
Tibia absent -- polydactyly -- arachnoid cyst N/A N/A No information
Megalencephaly -- polymicrogyria -- post-axial polydactyly -- hydrocephalus N/A N/A No information
Cephalopolysyndactyly N/A N/A No information
Greig Cephalopolysyndactyly Syndrome N/A N/A No information
Polysyndactyly -- trigonocephaly -- agenesis of corpus callosum N/A N/A No information
Corpus callosum agenesis -- polysyndactyly N/A N/A No information
Phocomelia -- thrombocytopenia -- encephalocele -- urogenital malformation N/A N/A No information
Micrencephaly corpus callosum agenesis N/A N/A No information
Oculo-cerebro-acral, (Roberts-like)-ectrodactyly N/A N/A No information
Cleft lip -- palate -- abnormal thumbs -- microcephaly N/A N/A No information
Neural tube defects X-linked N/A N/A No information
Spastic paraplegia with precocious puberty N/A N/A No information
Neural tube defect, folate-sensitive N/A N/A No information
Craniosynostosis -- alopecia -- brain defect N/A N/A No information
Axenfeld-Rieger anomaly with cardiac defects and sensorineural hearing loss N/A N/A No information
Glucose transport defect, blood-brain barrier N/A N/A No information
Short stature -- pituitary and cerebellar defects -- small sella turcica N/A N/A No information
Familial porencephaly N/A N/A No information
Holoprosencephaly -- ectrodactyly -- cleft lip/palate N/A N/A No information
Anophthalmia -- microcephaly -- hypogonadism N/A N/A No information
Cardiac malformation, cleft lip-palate, microcephaly and digital anomalies N/A N/A No information
Growth delay -- mental retardation -- mandibulofacial dysostosis -- microcephaly -- cleft palate N/A N/A No information
Dextrocardia -- microphthalmia -- cleft palate -- intellectual deficit N/A N/A No information
Dysraphism -- cleft lip palate -- limb reduction defects N/A N/A No information
Microbrachycephaly -- ptosis -- cleft lip N/A N/A No information
Meningeal angiomatosis -- cleft hypoplastic left heart N/A N/A No information
Pachygyria, frontotemporal N/A N/A No information
Microcephaly, corpus callosum dysgenesis and cleft lip-palate N/A N/A No information
Spastic paraparesis deafness N/A N/A No information
Distal hereditary motor neuropathy, type V N/A N/A No information
Lower motor neuron weakness N/A N/A No information
Upper motor neuron weakness N/A N/A No information
Amyloid Neuropathies N/A N/A No information
Cerebral Amyloid Angiopathy, Familial N/A N/A No information
Severe infantile axonal neuropathy N/A N/A No information
Adrenomyeloneuropathy N/A N/A No information
Neuropathy, distal hereditary motor N/A N/A No information
Neuropathy, distal hereditary motor, type VIIA N/A N/A No information
Polyradiculoneuropathy N/A N/A No information
Neuropathy, distal hereditary motor, type III N/A N/A No information
Neuropathy, Hereditary Sensory, Type II N/A N/A No information
Neuropathy, Hereditary Sensory and Autonomic Type I N/A N/A No information
Neuropathy, Hereditary Sensory, Type I N/A N/A No information
Congenital hypomyelination neuropathy N/A N/A No information
Corpus callosum agenesis-neuropathy N/A N/A No information
Giant axonal neuropathy N/A N/A No information
Leber hereditary optic neuropathy N/A N/A No information
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis N/A N/A No information
Myoclonic dystonia N/A N/A No information
Infantile axonal neuropathy N/A N/A No information
Spastic paraplegia -- neuropathy -- poikiloderma N/A N/A No information
Familial amyloid polyneuropathy N/A N/A No information
Optic neuropathy, anterior ischemic N/A N/A No information
Benign angiitis of the central nervous system N/A N/A No information
Caudal dysplasia sequence N/A N/A No information
Caudal regression syndrome N/A N/A No information
Holoprosencephaly -- caudal dysgenesis N/A N/A No information
Caudal appendage -- deafness N/A N/A No information
Caudal duplication N/A N/A No information
Facial paresis, hereditary, congenital N/A N/A No information
Kaufman oculocerebrofacial syndrome N/A N/A No information
Idiopathic double athetosis N/A N/A No information
Iris hypoplasia and glaucoma N/A N/A No information
Leukoencephalopathy -- palmoplantar keratoderma N/A N/A No information
Keratosis follicularis -- dwarfism -- cerebral atrophy N/A N/A No information
Acute cholinergic dysautonomia N/A N/A No information
Acute sensorineural hearing loss by acute acoustic trauma or sudden deafness or surgery induced acoustic trauma N/A N/A No information
Chediak-Higashi like syndrome N/A N/A No information
Absent corpus callosum -- cataract -- immunodeficiency N/A N/A No information
X-linked hydrocephalus spectrum N/A N/A No information
Torsion dystonia, autosomal dominant N/A N/A No information
Cataract -- ataxia -- deafness N/A N/A No information
Hereditary peripheral nervous disorder N/A N/A No information
Autoimmune limbic encephalitis N/A N/A No information
Epileptic encephalopathy, Lennox-Gastaut type N/A N/A No information
Coloboma of optic nerve N/A N/A No information
Hyperthermia induced defects N/A N/A No information
Thrombocytopenia -- cerebellar hypoplasia -- short stature N/A N/A No information
Corneal cerebellar syndrome N/A N/A No information
Polymicrogyria -- turricephaly -- hypogenitalism N/A N/A No information
Angioma hereditary neurocutaneous N/A N/A No information
Dysgraphia N/A N/A No information
Fahr's Syndrome N/A N/A No information
Gerstmann's Syndrome N/A N/A No information
Joubert Syndrome N/A N/A No information
Landau-Kleffner Syndrome N/A N/A No information
Megalencephaly N/A N/A No information
Melkersson-Rosenthal Syndrome N/A N/A No information
Miller Fisher Syndrome N/A N/A No information
Subacute Sclerosing Panencephalitis N/A N/A No information
Tardive Dyskinesia N/A N/A No information
Stiff-Person Syndrome N/A N/A No information
Cerebelloparenchymal autosomal recessive disorder 3 N/A N/A No information
Cerebelloparenchymal disorder 3 N/A N/A No information
Cerebelloparenchymal disorder V N/A N/A No information
Encephalopathy -- intracranial calcification -- growth hormone deficiency -- microcephaly -- retinal degeneration N/A N/A No information
L1 Syndrome N/A N/A No information
Trichothiodystrophy-neurocutaneous Syndrome N/A N/A No information
Trichothiodystrophy-neurotrichocutaneous Syndrome of Pollitt N/A N/A No information
Trichothiodystrophy, type C N/A N/A No information
Trichothiodystrophy -- sun sensitivity N/A N/A No information
Microcephaly -- glomerulonephritis -- Marfanoid habitus N/A N/A No information
Microcephalic primordial dwarfism, Toriello type N/A N/A No information
De Sanctis-Cacchione syndrome N/A N/A No information
HARD syndrome N/A N/A No information
Familial dysautonomia N/A N/A No information
Miller-Dieker syndrome N/A N/A No information
Diencephalic syndrome of infancy N/A N/A No information
Leigh syndrome N/A N/A No information
Xanthomatosis cerebrotendinous N/A N/A No information
Congenital hypoparathyroidism, seizures, growth and mental retardation and unusual facies N/A N/A No information
Aphasia, Broca N/A N/A No information
Auditory Diseases, Central N/A N/A No information
VACTERL hydrocephaly N/A N/A No information
VACTERL with hydrocephalus, X-linked N/A N/A No information
VACTERYL hydrocephaly N/A N/A No information
VACTERL association with hydrocephaly, X-linked N/A N/A No information
Alternating hemiplegia of childhood N/A N/A No information
Neurosyphilis -- asymptomatic N/A N/A No information
Thanatophoric dysplasia, type 2 N/A N/A No information
Thanatophoric dysplasia, type 1 N/A N/A No information
Osteogenesis imperfecta congenita, microcephaly, and cataracts N/A N/A No information
Francois dyscephalic syndrome N/A N/A No information
Oculocerebral syndrome with hypopigmentation N/A N/A No information
Cephalothoracic progressive lipodystrophy N/A N/A No information
Isaacs syndrome N/A N/A No information
Muscle-eye-brain syndrome N/A N/A No information
Parenchymatous cortical degeneration of cerebellum N/A N/A No information
Spinal intradural arachnoid cysts N/A N/A No information
Neurosyphilis -- tabes dorsalis N/A N/A No information
Spastic quadriplegia -- retinitis pigmentosa -- mental retardation N/A N/A No information
Spinal atrophy -- ophthalmoplegia -- pyramidal syndrome N/A N/A No information
Encephalopathy progressive -- optic atrophy N/A N/A No information
Spastic diplegia, infantile type N/A N/A No information
Macrocephaly, mental retardation, short stature, spastic paraplegia and CNS malformations N/A N/A No information
Digitorenocerebral syndrome N/A N/A No information
Microcephaly -- deafness syndrome N/A N/A No information
Multiple sclerosis -- ichthyosis -- factor 8 deficiency N/A N/A No information
Recurrent peripheral facial palsy N/A N/A No information
Nova syndrome N/A N/A No information
Polyneuropathy -- mental retardation -- acromicria -- premature menopause N/A N/A No information
Knuckle pads, leukonychia and sensorineural deafness N/A N/A No information
Lysteria monocytoigeneses meningitis N/A N/A No information
Hyperphagia N/A N/A No information
Myoclonus-ataxia N/A N/A No information
Oculocerebral hypopigmentation syndrome, type Preus N/A N/A No information
Oculorenocerebellar syndrome N/A N/A No information
Cerebro oculo genital syndrome N/A N/A No information
Neurofaciodigitorenal syndrome N/A N/A No information
Microcephalic osteodysplastic primordial dwarfism, type 2 N/A N/A No information
Microcephalic osteodysplastic primordial dwarfism, type 3 N/A N/A No information
Septooptic dysplasia -- digital anomalies N/A N/A No information
Microcephaly -- microphthalmos -- blindness N/A N/A No information
Paraneoplastic Neurologic Disorders N/A N/A No information
Rasmussen subacute encephalitis N/A N/A No information
Spastic paresis -- glaucoma -- mental retardation N/A N/A No information
Microcornea -- glaucoma -- absent frontal sinuses N/A N/A No information
Spastic paraplegia with Kallmann syndrome N/A N/A No information
Nivelon-Nivelon-Mabille syndrome N/A N/A No information
Ectodermal dysplasia -- mental retardation -- CNS malformation N/A N/A No information
Macrogyria, pseudobulbar palsy and mental retardation N/A N/A No information
Dinno-Shearer-Weisskopf syndrome N/A N/A No information
Ectodermal dysplasia -- neurosensory deafness N/A N/A No information
Hemimegalencephaly N/A N/A No information
Meningoencephalocele N/A N/A No information
Sacral plexopathy N/A N/A No information
Optic nerve disorder N/A N/A No information
Neuritis with brachial predilection N/A N/A No information
Microcephaly, Amish type N/A N/A No information
Multifocal heterotopia N/A N/A No information
Subcortical laminar heterotopia N/A N/A No information
Marginal glioneuronal heterotopia N/A N/A No information
Periventricular laminar heterotopia N/A N/A No information
Heterotopia, periventricular, autosomal recessive N/A N/A No information
Hereditary nodular heterotopia N/A N/A No information
Subependymal nodular heterotopia N/A N/A No information
Familial band heterotopia N/A N/A No information
Iris coloboma, macrocephaly, agenesis of the corpus callosum, brachydactyly and mental retardation N/A N/A No information
Agenesis of the corpus callosum -- mental retardation -- coloboma -- micrognathia N/A N/A No information
Granulomas, congenital cerebral N/A N/A No information
Frontotemporal dementia, ubiquitin-positive N/A N/A No information
Arachnodactyly -- ataxia -- cataract -- aminoaciduria -- mental retardation N/A N/A No information
Cerebellum agenesis -- hydrocephaly N/A N/A No information
Accessory deep peroneal nerve N/A N/A No information
Common peroneal nerve dysfunction N/A N/A No information
Synovitis granulomatous with uveitis and cranial neuropathies N/A N/A No information
Leukoencephalopathy -- metaphyseal chondrodysplasia N/A N/A No information
Unusual facies, skeletal abnormalities, communicating hydrocephalus N/A N/A No information
Encephalopathy, familial, with neuroserpin inclusion bodies N/A N/A No information
Lethal arthrogryposis with anterior horn cell disease (LAAHD) N/A N/A No information
Neuronopathy, distal hereditary motor, type IIB N/A N/A No information
Holoprosencephaly, recurrent infections, and monocytosis N/A N/A No information
Acroparesthesia syndrome N/A N/A No information
Hemorrhagic shock and encephalopathy syndrome N/A N/A No information
Corpus callosum agenesis -- blepharophimosis -- Robin sequence N/A N/A No information
Microcephaly micropenis convulsions N/A N/A No information
Multiple system atrophy (MSA) with orthostatic hypotension N/A N/A No information
Alopecia, epilepsy, pyorrhea, mental subnormality N/A N/A No information
Encephalocele anterior N/A N/A No information
Exencephaly N/A N/A No information
Acroosteolysis neurogenic N/A N/A No information
Degenerative motor system disease N/A N/A No information
Bone fragility, craniosynostosis, proptosis, hydrocephalus N/A N/A No information
Neuroferritinopathy N/A N/A No information
Neuroferritinopathy (adult-onset basal ganglia disease) N/A N/A No information
Basal Ganglia Disease, Adult-Onset N/A N/A No information
Macrocephaly -- short stature -- paraplegia N/A N/A No information
Microcephaly brachydactyly kyphoscoliosis N/A N/A No information
Hydrocephalus -- growth delay -- skeletal anomalies N/A N/A No information
Opthalmoplegia ataxia hypoacusis N/A N/A No information
Corpus callosum dysgenesis hypopituitarism N/A N/A No information
Agyria-pachygyria type 1 N/A N/A No information
Anterior spinal artery stroke N/A N/A No information
Anterior cord syndrome N/A N/A No information
Anterior spinal artery syndrome N/A N/A No information
Anticholinergic syndrome N/A N/A No information
Apallic syndrome N/A N/A No information
Hypomyelination -- congenital cataract N/A N/A No information
Adversive syndrome N/A N/A No information
Visceral neuropathy, familial, autosomal dominant N/A N/A No information
Grahmann's syndrome N/A N/A No information
Hunter-MacDonald syndrome N/A N/A No information
Unusual facies, oligodontia and precocious choroid calcifications N/A N/A No information
Hypomyelination -- hypogonadotropic hypogonadism -- hypodontia N/A N/A No information
Oligodontia, microcephaly, short stature and characteristic facies N/A N/A No information
Oligodontia and congenital sensorineural hearing loss N/A N/A No information
Intercostal nerve syndrome N/A N/A No information
Fochs-LADD N/A N/A No information
Basal ganglia disease, biotin-responsive N/A N/A No information
Bannwarth's triad N/A N/A No information
Rhombencephalosynapsis N/A N/A No information
Autonomic Dysreflexia N/A N/A No information
Vestibulocochlear Nerve Diseases N/A N/A No information
Central pontine myelinolysis N/A N/A No information
Mc Leod neuroacanthocytosis syndrome N/A N/A No information
Hereditary vascular retinopathie -- Raynaud phenomenon -- migraine N/A N/A No information
Hydrocephaly low insertion umbilicus N/A N/A No information
Angioneurotic Edema N/A N/A No information
Craniorachischisis N/A N/A No information
Syringomelia N/A N/A No information
Neurosyphilis -- meningovascular N/A N/A No information
Lymphoedema -- cerebral arteriovenous anomaly N/A N/A No information
Limbic encephalitis -- neuromyotonia -- hyperhidrosis -- polyneuropathy N/A N/A No information
BAER N/A N/A No information
Monomelic Amyotrophy N/A N/A No information
Neuroleptic Malignant Syndrome N/A N/A No information
Ohtahara Syndrome N/A N/A No information
Pelizaeus-Merzbacher Disease N/A N/A No information
Pick's Disease N/A N/A No information
Sandhoff Disease N/A N/A No information
Schilder's Disease N/A N/A No information
Septo-Optic Dysplasia N/A N/A No information
Shaken Baby Syndrome N/A N/A No information
Shy-Drager Syndrome N/A N/A No information
Sturge-Weber Syndrome N/A N/A No information
Todd's Paralysis N/A N/A No information
Wallenberg's Syndrome N/A N/A No information
Neuromyotonia N/A N/A No information
Neuromyelitis Optica N/A N/A No information
Intracranial arachnoid cysts N/A N/A No information
Wernicke's encephalopathy N/A N/A No information
Wernicke-Korsakoff syndrome N/A N/A No information
Meralgia paresthetica N/A N/A No information
Cervical Spondylosis N/A N/A No information
Morton's Neuroma N/A N/A No information
Brachial Neuritis N/A N/A No information
Myokymia N/A N/A No information
Cadasil N/A N/A No information
Gliosis N/A N/A No information
Cauda equina syndrome N/A N/A No information
Adies Syndrome N/A N/A No information
GSS N/A N/A No information
Moyamoya Syndrome N/A N/A No information
Frey Syndrome N/A N/A No information
Walker-Warburg Syndrome N/A N/A No information
Hyperekplexia N/A N/A No information
Osteopaenia -- myopia -- hearing loss -- intellectual deficit -- facial dysmorphism N/A N/A No information
Polyglucosan body disease, adult N/A N/A No information
Renal dysplasia hepatic fibrosis dandy walker N/A N/A No information
Seizures mental retardation hair dysplasia N/A N/A No information
Sensorineural hearing loss, early greying, and essential tremor N/A N/A No information
Polyneuropathy -- Ophthalmoplegia -- Leukoencehalopathy -- Intestinal Pseudo-Obstruction N/A N/A No information
Hyperkinetic dysarthria N/A N/A No information
Tetrahydrobiopterin deficiencies N/A N/A No information
Spastic dysarthria N/A N/A No information
Adult Polyglucosan Body Disease N/A N/A No information
Congenital Bilateral Perisylvian Syndrome N/A N/A No information
Kuf Disease N/A N/A No information
Syringobulbia N/A N/A No information
Kluver-Bucy Syndrome N/A N/A No information
Kernicterus N/A N/A No information
Horner Syndrome N/A N/A No information
Tetrahydrobiopterin Deficiency N/A N/A No information
Binswanger Disease N/A N/A No information
Cerebrorenodigital syndrome N/A N/A No information
Diencephalic Syndrome N/A N/A No information
Infantile Neuroaxonal Dystrophy N/A N/A No information
Mulibrey Nanism syndrome N/A N/A No information
Vogt-Koyanagi-Harada Syndrome N/A N/A No information
Schinzel Giedion Syndrome N/A N/A No information
Acrocallosal Syndrome (Schinzel Type) N/A N/A No information
Selected Encephalitides N/A N/A No information
Lowe Syndrome N/A N/A No information
Cerebrocostomandibular Syndrome N/A N/A No information
Kleine-Levin Syndrome N/A N/A No information
MULIBREY Nanism N/A N/A No information
Pallister-Hall Syndrome N/A N/A No information
Choroido cerebral calcification syndrome infantile form N/A N/A No information
Thalamic Syndrome (Dejerine Roussy) N/A N/A No information
Chondrodysplasia -- pseudohermaphrodism N/A N/A No information
Revesz Debuse syndrome N/A N/A No information
Neuronal intranuclear hyaline inclusion disease N/A N/A No information
Retinopathy -- anaemia- CNS anomalies N/A N/A No information
Revesz Syndrome N/A N/A No information
Ophtalmoplegia -- ataxia -- hypoacusis N/A N/A No information
Hing Torack Dowston syndrome N/A N/A No information
Aniridia ataxia renal agenesis psychomotor retardation N/A N/A No information
Braddock Jones Superneau syndrome N/A N/A No information
Thyrocerebral-retinal syndrome N/A N/A No information
Moebius sequence N/A N/A No information
Moebius syndrome 1 N/A N/A No information
Moebius Syndrome N/A N/A No information
Nevi -- atrial myxoma -- myxoid neurofibromata -- ephelides N/A N/A No information
Wright dick syndrome N/A N/A No information
Acrocallosal syndrome N/A N/A No information
Pantothenate kinase-associated neurodegeneration N/A N/A No information
PEHO-like syndrome N/A N/A No information
Bonnemann-Meinecke-Reich syndrome N/A N/A No information
Dancing Eye syndrome N/A N/A No information
Glaucoma ectopia microspherophakia stiff joints short stature N/A N/A No information
Down's Syndrome associated Alzheimer's disease N/A N/A No information
Human HOXA1 Syndromes N/A N/A No information
Cruse Syndrome N/A N/A No information
Jequier-Deonna Syndrome N/A N/A No information
Robinson syndrome N/A N/A No information
Pick's disease of the brain N/A N/A No information
CAR syndrome N/A N/A No information
Cerebro-oculo-nasal syndrome N/A N/A No information
Craniofacial conodysplasia N/A N/A No information
Cutaneomeningospinal angiomatosis N/A N/A No information
FOSMN syndrome N/A N/A No information
Frey's syndrome N/A N/A No information
Fried syndrome N/A N/A No information
Goossens-Devriendt syndrome N/A N/A No information
Schwartz newark syndrome N/A N/A No information
Right hemisphere syndrome N/A N/A No information
Rimbaud-Passouant-Vallat syndrome N/A N/A No information
Rot-Bernhardt syndrome N/A N/A No information
Strauss syndrome N/A N/A No information
Superior orbital fissure syndrome N/A N/A No information
Todd paralysis N/A N/A No information
Traumatic spreading depression syndrome N/A N/A No information
Uhthoff syndrome N/A N/A No information
Vail syndrome N/A N/A No information
Zanoli-Vecchi syndrome N/A N/A No information
ADANE N/A N/A No information
Stiff baby syndrome N/A N/A No information
Fryns-Aftimos syndrome N/A N/A No information
Fryns macrocephaly N/A N/A No information
XLAG syndrome N/A N/A No information
Axenfeld-Rieger anomaly -- hydrocephaly -- skeletal abnormalities N/A N/A No information
Benson's syndrome N/A N/A No information
Haenel syndrome N/A N/A No information
Heidenhain syndrome N/A N/A No information
Henkin syndrome N/A N/A No information
Hoigne syndrome N/A N/A No information
Holmes syndrome N/A N/A No information
Homen syndrome N/A N/A No information
Howship-Romberg syndrome N/A N/A No information
Jirasek-Zuelzer-Wilson syndrome N/A N/A No information
Keutel syndrome 2 N/A N/A No information
Temporal lobectomy behavior syndrome N/A N/A No information
Kramer-Pollnow disease N/A N/A No information
Krause syndrome N/A N/A No information
Kreibig opticomalacia N/A N/A No information
Lhermitte-Cornil-Quesnel syndrome N/A N/A No information
Lhermitte-McAlpine syndrome N/A N/A No information
Lissauer paralysis N/A N/A No information
Mann syndrome N/A N/A No information
Nothnagel acroparesthesia N/A N/A No information
Obal syndrome N/A N/A No information
Osuntokun syndrome N/A N/A No information
Postconcussive syndrome N/A N/A No information
Putti-Chavany syndrome N/A N/A No information
Hydrocephalus -- growth retardation -- skeletal anomalies N/A N/A No information
CACH syndrome N/A N/A No information
Cennamo-Gangemi syndrome N/A N/A No information
Apraxia, Ideomotor N/A N/A No information
Dandy-Walker variant N/A N/A No information
Hemifacial atrophy agenesis of the caudate nucleus N/A N/A No information
Eijkman's syndrome N/A N/A No information
Double cortex syndrome N/A N/A No information
Basilar impression primary N/A N/A No information
Colloid cysts of third ventricle N/A N/A No information
Burnett-Schwartz-Berberian syndrome N/A N/A No information
Hydrocephalus -- craniosynostosis -- bifid nose N/A N/A No information
CANOMAD syndrome N/A N/A No information
BANF acoustic neurinoma N/A N/A No information
Cree leukoencephalopathy N/A N/A No information
Genoa syndrome N/A N/A No information
Calloso-genital dysplasia N/A N/A No information
Hutterite cerebroosteonephrodysplasia syndrome N/A N/A No information
Schwannomatosis N/A N/A No information
Chitayat-Moore-Del Bigio syndrome N/A N/A No information
Esthesioneuroblastoma N/A N/A No information
Choroid plexus cyst N/A N/A No information
Hurst-Hallam-Hockey syndrome N/A N/A No information
Cerebrorenodigital syndrome with limb malformations and triradiate acetabula N/A N/A No information
Choreoacanthocytosis amyotrophic N/A N/A No information
Leukomalacia N/A N/A No information
Dentatorubral pallidoluysian disorder N/A N/A No information
Argyll-Robertson syndrome N/A N/A No information
Avellis's syndrome N/A N/A No information
Babinski-Nageotte syndrome N/A N/A No information
Balint's syndrome N/A N/A No information
Basilar artery insufficiency syndrome N/A N/A No information
Benedikt's syndrome N/A N/A No information
Bianchi's syndrome N/A N/A No information
Bing-Neel syndrome N/A N/A No information
Bonnier's syndrome N/A N/A No information
Bristowe's syndrome N/A N/A No information
Brun's syndrome N/A N/A No information
Catatonic syndrome N/A N/A No information
Alien hand syndrome N/A N/A No information
Austrian syndrome N/A N/A No information
Autonomic dysreflexia syndrome N/A N/A No information
Bald soprano syndrome N/A N/A No information
Barsony-Polgar syndrome 1 N/A N/A No information
Bartschi-Rochaix syndrome N/A N/A No information
Bell mania N/A N/A No information
Berger paresthesia N/A N/A No information
Bessman-Baldwin syndrome N/A N/A No information
Billroth disease (1) N/A N/A No information
Borries syndrome N/A N/A No information
Bradbury-Eggleston syndrome N/A N/A No information
Brain Fag syndrome N/A N/A No information
Brissaud-Marie syndrome N/A N/A No information
Brown-Symmers disease N/A N/A No information
Bruns-Garland syndrome N/A N/A No information
Dana syndrome N/A N/A No information
Disequilibrium syndrome N/A N/A No information
FACWA syndrome N/A N/A No information
Fanconi-Albertini-Zellweger syndrome N/A N/A No information
Fanconi-Turler syndrome N/A N/A No information
Foix-Alajouanine syndrome N/A N/A No information
Gerlier disease N/A N/A No information
Hydrocephalus due to congenital stenosis of aqueduct of sylvius N/A N/A No information
Paroxysmal kinesigenic choreoathetosis N/A N/A No information
Saal-Bulas syndrome N/A N/A No information
Micro syndrome N/A N/A No information
Schwartz, Cohen-Addad, Lambert syndrome N/A N/A No information
Southwestern Athabaskan genetic diseases N/A N/A No information
Granulomatous Angiitis of the Central Nervous System N/A N/A No information
Muller-Barth-Menger syndrome N/A N/A No information
Temtamy syndrome N/A N/A No information
Hoyeraal-Hreidarsson syndrome N/A N/A No information
Navajo neurohepatopathy N/A N/A No information
MN1 N/A N/A No information
Diastematomyelia N/A N/A No information
Megalencephaly -- cutis marmorata telangiectatica congenita N/A N/A No information
Spondylocostal dysostosis, Dandy-Walker N/A N/A No information
Fitzsimmons-Walson-Mellor syndrome N/A N/A No information
Hashimoto's encephalitis N/A N/A No information
Massa-Casaer-Ceulemans syndrome N/A N/A No information
Corpus callosum agenesis -- double urinary collecting system N/A N/A No information
Striatonigral degeneration infantile N/A N/A No information
Tome-Brune-Fardeau syndrome N/A N/A No information
Phacomatosis pigmentokeratotica N/A N/A No information
Jung-Wolff-Back-Stahl syndrome N/A N/A No information
Papilloma of choroid plexus N/A N/A No information
Microcephaly -- hypergonadotropic hypogonadism -- short stature N/A N/A No information
Mousa-Al Din-Al Nassar syndrome N/A N/A No information
Plum syndrome N/A N/A No information
Osteosclerosis, abnormalities of nervous system and meninges N/A N/A No information
Neuroectodermal endocrine syndrome N/A N/A No information
Neuronal intranuclear inclusion disease N/A N/A No information
Cerebro oculo skeleto renal syndrome N/A N/A No information
Powell-Venencie-Gordon syndrome N/A N/A No information
Focal alopecia congenital -- megalencephaly N/A N/A No information
Megalencephalic leukoencephalopathy with subcortical cysts N/A N/A No information
Cutler-Bass-Romshe syndrome N/A N/A No information
Tang Hsi Ryu syndrome N/A N/A No information
Dandy-Walker -- facial hemangioma N/A N/A No information
Proud-Levine-Carpenter syndrome N/A N/A No information
Lurie-Kletsky syndrome N/A N/A No information
Pili torti -- developmental delay -- neurological abnormalities N/A N/A No information
Facial asymetry -- temporal seizures N/A N/A No information
Harding ataxia N/A N/A No information
Luteinizing hormone releasing hormone, deficiency of, with ataxia N/A N/A No information
Guam disease N/A N/A No information
Dysplastic cortical hyperostosis N/A N/A No information
Morse-Rawnsley-Sargent syndrome N/A N/A No information
COACH syndrome N/A N/A No information
Cyprus facial neuromusculoskeletal syndrome N/A N/A No information
Arena syndrome N/A N/A No information
Athabaskan brainstem dysgenesis N/A N/A No information
Arima syndrome N/A N/A No information
Dionisi-Vici-Sabetta-Gambarara syndrome N/A N/A No information
Oculo cerebro acral syndrome N/A N/A No information
Retinopathy -- anemia -- CNS anomalies N/A N/A No information
Steinfeld syndrome N/A N/A No information
Cerebral gigantism -- jaw cysts N/A N/A No information
Posterior column ataxia with retinitis pigmentosa N/A N/A No information
Bahemuka Brown syndrome N/A N/A No information
Mohr-Tranebjaerg syndrome N/A N/A No information
Palmer-Pagon syndrome N/A N/A No information
Susac syndrome N/A N/A No information
Kasznica-Carlson-Coppedge syndrome N/A N/A No information
Ferlini-Ragno-Calzolari syndrome N/A N/A No information
Dincsoy-Salih-Patel syndrome N/A N/A No information
Daentl-Towsend-Siegel syndrome N/A N/A No information
Idiopathic hypereosinophilic syndrome N/A N/A No information
Neuhauser-Eichner-Opitz syndrome N/A N/A No information
Paraneoplastic cerebellar degeneration N/A N/A No information
Spranger-Schinzel-Myers syndrome N/A N/A No information
Notalgia paresthetica N/A N/A No information
Telencephalic leukoencephalopathy N/A N/A No information
Pallidopyramidal syndrome N/A N/A No information
Seow-Najjar syndrome N/A N/A No information
Podder-Tolmie syndrome N/A N/A No information
Telfer-Sugar-Jaeger syndrome N/A N/A No information
Flynn-Aird syndrome N/A N/A No information
Tarlov cysts N/A N/A No information
Arakawa syndrome 1 N/A N/A No information
Perisylvian syndrome N/A N/A No information
Brown-Vialetto-Van Laere syndrome N/A N/A No information
Sylvester (P.E.) syndrome N/A N/A No information
Brain -- bone -- fat N/A N/A No information
Encephalitis lethargica N/A N/A No information
Acrofacial dysostosis Rodriguez type N/A N/A No information
Colpocephaly N/A N/A No information
Acromelic frontonasal dysplasia N/A N/A No information
BOR-Duane hydrocephalus contiguous gene syndrome N/A N/A No information
Beemer-Ertbruggen syndrome N/A N/A No information
Boylan-Dew-Greco syndrome N/A N/A No information
Avasthey syndrome N/A N/A No information
Baker-Vinters syndrome N/A N/A No information
De Grouchy Syndrome N/A N/A No information
Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus N/A N/A No information
Bonneman-Meinecke-Reich syndrome N/A N/A No information
Grand-Kaine-Fulling syndrome N/A N/A No information
Ben-Ari-Shuper-Mimouni syndrome N/A N/A No information
Cerebro-oculo-dento-auriculo-skeletal syndrome N/A N/A No information
Baraitser Brett Piesowicz syndrome N/A N/A No information
PHACE association N/A N/A No information
Fitzsimmons-Guilbert syndrome N/A N/A No information
Roy-Maroteaux-Kremp syndrome N/A N/A No information
Craniotelencephalic dysplasia N/A N/A No information
Boucher-Neuhauser syndrome N/A N/A No information
Kuru syndrome N/A N/A No information
Synovitis granulomatous with uveitis and cranial neuropathies, familial N/A N/A No information
Alopecia, epilepsy, oligophrenia syndrome of Moynahan N/A N/A No information
Arakawa's syndrome 2 N/A N/A No information
Westphal-Piltz pupil N/A N/A No information
Lafora disease N/A N/A No information
Groll-Hirschowitz syndrome N/A N/A No information
Kohlschutter-Tonz syndrome N/A N/A No information
Nielsen-Jacobs syndrome N/A N/A No information
Erythrokeratodermia ataxia N/A N/A No information
Fisher (M.) syndrome N/A N/A No information
Severe achondroplasia with developmental delay and acanthosis nigricans N/A N/A No information
Turcot syndrome N/A N/A No information
Becker disease N/A N/A No information
Delleman-Oorthuys syndrome N/A N/A No information
Fothergill disease N/A N/A No information
Jumping Frenchmen of Maine N/A N/A No information
Marie type ataxia N/A N/A No information
Leigh syndrome, French Canadian type N/A N/A No information
Meige syndrome N/A N/A No information
Craniodiaphyseal dysplasia N/A N/A No information
Hyperexplexia N/A N/A No information
Gelineau's syndrome N/A N/A No information
Sneddon Syndrome N/A N/A No information
Pelizaeus-Merzbacher disease, recessive, acute infantile N/A N/A No information
Pelizaeus-Merzbacher brain sclerosis N/A N/A No information
Whole-body acute irradiation -- cerebral syndrome N/A N/A No information
Levine-Critchley syndrome N/A N/A No information
Erythrokeratodermia with ataxia N/A N/A No information
Lowe oculocerebrorenal syndrome N/A N/A No information
Ramsay Hunt Syndrome type I N/A N/A No information
Parsonage Turner syndrome N/A N/A No information
Devic disease N/A N/A No information
Absence of septum pellucidum and septo-optic dysplasia N/A N/A No information
Mononeuritis multiplex N/A N/A No information
Young McKeever Squier syndrome N/A N/A No information
XK aprosencephaly N/A N/A No information
Wiedemann Grosse Dibbern syndrome N/A N/A No information
Wright Dyck syndrome N/A N/A No information
Waterhouse-Friderichsen syndrome N/A N/A No information
Worster Drought syndrome N/A N/A No information
Wallerian degeneration N/A N/A No information
Von voss Cherstvoy syndrome N/A N/A No information
Wells Jankovic syndrome N/A N/A No information
Warburg Sjo Fledelius syndrome N/A N/A No information
Zunich neuroectodermal syndrome N/A N/A No information
Ivemark III N/A N/A No information
Sabin-Feldman syndrome N/A N/A No information
Penfield syndrome N/A N/A No information
Westphal-Leyden ataxia N/A N/A No information
Currarino triad N/A N/A No information
Lhermitte-Duclos disease N/A N/A No information
Microcephaly, holoprosencephaly, and intrauterine growth retardation N/A N/A No information
Knobloch syndrome N/A N/A No information
Jensen syndrome N/A N/A No information
Meretoja syndrome N/A N/A No information
Barre-Lieou syndrome N/A N/A No information
Fazio-Londe syndrome N/A N/A No information
Silverman-Handmaker syndrome N/A N/A No information
King-Denborough syndrome N/A N/A No information
Kelley-Seegmiller syndrome N/A N/A No information
Chavany-Brunhes syndrome N/A N/A No information
Occult spinal dysraphism N/A N/A No information
Limb-body wall complex N/A N/A No information
Nevus sebaceous of Jadassohn N/A N/A No information
Encephalo cranio cutaneous lipomatosis N/A N/A No information
Neurocutaneous melanosis N/A N/A No information
Hydrolethalus syndrome N/A N/A No information
Van Maldergem Wetzburger Verloes syndrome N/A N/A No information
Ausrian triad N/A N/A No information
Vein of Galen aneurysm N/A N/A No information
Bobble-head doll syndrome N/A N/A No information
Familial chronic infantile diffuse sclerosis N/A N/A No information
Behr syndrome N/A N/A No information
NAME syndrome N/A N/A No information
Balo's concentric sclerosis N/A N/A No information
Warfarin syndrome N/A N/A No information
Corpus callosum agenesis N/A N/A No information
Maternally Inherited Leigh Syndrome N/A N/A No information
Riley Shwachman syndrome N/A N/A No information
Pelizaeus-Merzbacher disease, adult onset N/A N/A No information
Marchiafava-Bignami disease N/A N/A No information

Types of Nervous system conditions

For more information about types of Nervous system conditions, refer to our section on types of Nervous system conditions.

About incidence:

The medical term 'incidence' of Nervous system conditions usually refers to the annual diagnosis rate of new cases of Nervous system conditions. Prevalence is a different medical disease measure that refers to the estimated population of people who are managing Nervous system conditions at any given time (e.g. prevalence includes people who have had a medical condition for a long time). For more information on prevalence and incidence statistics, see about prevalence and incidence statistics.



Footnotes:
1. Pathophysiology of Disease, Stephen J. McPhee, Vishwanash R. Lingappa, Willim F. Ganong, Jack D. Lang, Prentice Hall, 1995
 

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