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Diseases » Brain conditions » Deaths
 

Death Statistics for Types of Brain conditions

Deaths and Brain conditions:

This section presents information about the death rate statistics for the various types of Brain conditions.

Death Statistics for Types of Brain conditions

Disease

Death Rate Estimate

US deaths estimate

Statistic Used for Calculation

concussion N/A N/A No information
Acute Disseminated Encephalomyelitis N/A N/A No information
Adrenoleukodystrophy N/A N/A 1 per 20,000 people suffer from X-linked adrenoleukodystrophy, Genetics Home reference website
Adult-onset ALD N/A N/A No information
Agenesis of the corpus callosum N/A N/A rare
Agnosia N/A N/A rare
Aicardi syndrome N/A N/A rare
Alexander Syndrome N/A N/A rare
Alpers Syndrome N/A N/A rare
Alternating Hemiplegia N/A N/A rare
Alveolar Hydatid Disease N/A N/A No information
Alzheimer's Disease approx 1 in 68 or 1.47% or 4 million people in USA more than 4 million Americans (CDC); estimated 4 million people in the U.S (NHWIC) more than 4 million Americans (CDC); estimated 4 million people in the U.S (NHWIC)
Amnesia N/A N/A No information
Amnesic shellfish poisoning N/A N/A No information
Amnestic disorder N/A N/A No information
Anencephaly N/A N/A No information
Angelman syndrome N/A N/A 1 per 12,000 - 20,000 people are affected by Angelman syndrome, Genetics Home Reference website
Anoxia N/A N/A No information
Aphasia N/A N/A 1 million Americans (NINDS)
Apraxia N/A N/A No information
Arachnoid Cysts N/A N/A No information
Arachnoiditis N/A N/A No information
Arteriovenous Malformation N/A N/A No information
Asperger syndrome N/A N/A No information
Ataxia Telangiectasia N/A N/A 1 per 40,000 - 100,000 people worldwide suffer from ataxia-telangiectasia, Genetics Home Reference website
Attention Deficit Hyperactivity Disorder N/A N/A 3.3 million children have ADD in USA (NHIS-97); estimated 2 million American children; 3 to 5 percent of all children (NIMH).
Auditory Processing Disorder N/A N/A No information
Autism N/A N/A 1 in 500 to 1 in 2,500 (NIMH); 1-in-1000 to 2-in-1000, depending on diagnostic criteria
Bacterial meningitis N/A N/A No information
Balance disorders N/A N/A No information
Binswanger's Disease N/A N/A rare
Bipolar disorder N/A N/A 1.2 percent of the population; 2.3 million adult Americans (NIMH)
Bovine spongiform encephalopathy N/A N/A No information
Brain abscess N/A N/A No information
Brain cancer unavailable No information
Brain compression N/A N/A No information
Brain damage N/A N/A No information
Canavan disease N/A N/A 1 per 6,400 - 13,500 people of Ashkenazi Jewish heritage suffer from Canavan disease, Genetics Home Reference website
Central Pain Syndrome N/A N/A No information
Cephalic disorders N/A N/A No information
Cephalic tetanus N/A N/A No information
Cerebral Aneurysm N/A N/A No information
Cerebral Arteriosclerosis N/A N/A No information
Cerebral Atrophy N/A N/A No information
Cerebral hemorrhage N/A N/A No information
Cerebral Palsy N/A N/A No information
Cerebrovascular Conditions approx 1 in 33 or 3.00% or 8.2 million people in USA 30 per 1000 - NHIS95 30 per 1000 - NHIS95
Chiari Malformation N/A N/A No information
Chorea N/A N/A No information
Chronic wasting disease (CWD) of mule deer and elk N/A N/A No information
Classic childhood ALD N/A N/A No information
Coma N/A N/A No information
Convulsions N/A N/A No information
Corticobasal Degeneration N/A N/A No information
Craniosynostosis N/A N/A No information
Creutzfeldt-Jakob Disease N/A N/A No information
Cryptococcal Meningitis N/A N/A No information
Dandy-Walker Syndrome N/A N/A No information
Delirium N/A N/A No information
Dementia N/A N/A No information
Dementia With Lewy Bodies N/A N/A No information
Dysgraphia N/A N/A No information
Dyslexia N/A N/A No information
Dystonias N/A N/A No information
Eastern equine encephalitis N/A N/A No information
Empty Sella Syndrome N/A N/A rare
Encephalitis N/A N/A No information
Encephalitis, California serogroup viral N/A N/A No information
Encephaloceles N/A N/A rare
Epilepsy N/A N/A 2.3 million Americans (CDC)
Fahr's Syndrome N/A N/A rare
Fatal familial insomnia N/A N/A No information
Febrile Seizures N/A N/A No information
Feline spongiform encephalopathy N/A N/A No information
Female carrier ALD N/A N/A No information
Fetal alcohol syndrome N/A N/A No information
Friedreich's ataxia N/A N/A No information
Gaucher Disease N/A N/A 1 per 50,000 - 100,000 people are affected by Gaucher disease, Genetics Home Reference website
Gerstmann's Syndrome N/A N/A No information
GSS (Gerstmann Sträussler Syndrome) N/A N/A No information
Head injury N/A N/A No information
Hemangioblastoma N/A N/A No information
High altitude cerebral edema N/A N/A No information
Holoprosencephaly N/A N/A No information
Huntington's Disease N/A N/A estimated 3-7 per 100,000 people of European ancestry suffer from Huntington disease, Genetics Home Reference website
Hydranencephaly N/A N/A rare
Hydrocephalus N/A N/A No information
Infantile Refsum Disease N/A N/A No information
Joubert Syndrome N/A N/A rare
Korsakoff's psychosis N/A N/A No information
Krabbé Disease N/A N/A rare
Kuru N/A N/A No information
Landau-Kleffner Syndrome N/A N/A rare
Leukodystrophy N/A N/A No information
Megalencephaly N/A N/A No information
MELAS N/A N/A No information
Melkersson-Rosenthal Syndrome N/A N/A No information
Meningioma N/A N/A No information
Meningitis unavailable No information
Meningococcal disease unavailable No information
Mental illness N/A N/A No information
Metachromatic Leukodystrophy N/A N/A No information
Microcephaly N/A N/A rare
Moyamoya Disease N/A N/A rare
Multi-Infarct Dementia N/A N/A No information
Multiple Sclerosis N/A N/A 1-in-700 (NIAID)
Murray Valley encephalitis N/A N/A No information
Myoclonus N/A N/A No information
Narcolepsy N/A N/A 200,000 Americans (NHLBI estimate); 50,000 diagnosed.
Neural tube defect N/A N/A No information
Neuroblastoma N/A N/A No information
Neurocysticercosis N/A N/A No information
Neuroleptic Malignant Syndrome N/A N/A No information
Neuronal Migration Disorders N/A N/A No information
Ohtahara Syndrome N/A N/A No information
Olivopontocerebellar Atrophy N/A N/A No information
Opsoclonus Myoclonus N/A N/A No information
Parkinson's Disease approx 1 in 272 or 0.37% or 1 million people in USA 1 million people (unreliable estimate) 1 million people (unreliable estimate)
Pelizaeus-Merzbacher Disease N/A N/A rare
Persistent Vegetative State N/A N/A No information
Pick's Disease N/A N/A No information
Porencephaly N/A N/A extremely rare
Progressive Multifocal Leukoencephalopathy N/A N/A No information
Progressive Supranuclear Palsy N/A N/A rare
Pseudotumor Cerebri N/A N/A about 1-2 people per 100,000 population have benign intracranial hypertension in the US (Association for Spina Bifida and Hydrocephalus)
Rabies unavailable No information
Rasmussen's Encephalitis N/A N/A rare
Refsum Disease N/A N/A No information
Rett's syndrome N/A N/A estimated 1 per 10,000 - 22,000 females suffer from Rett syndrome, Genetics Home Reference website
Schizencephaly N/A N/A extremely rare
Schizophrenia N/A N/A Approximately 2.2 million American adults (NIMH); estimated 1.3% adults (USSG); more than 2 million Americans
Septo-Optic Dysplasia N/A N/A rare
Shaken Baby Syndrome N/A N/A No information
Soto's Syndrome N/A N/A rare
Spastic disorders N/A N/A No information
St. Louis encephalitis N/A N/A No information
Stroke approx 1 in 59 or 1.69% or 4.6 million people in USA estimated 4.6 million (NHLBI) estimated 4.6 million (NHLBI)
Subacute Sclerosing Panencephalitis N/A N/A rare - because of the rarity of measles due to vaccination programs.
Subarachnoid hemorrhage N/A N/A No information
Subdural hematoma N/A N/A No information
Sydenham chorea N/A N/A No information
Tapeworms N/A N/A No information
Tardive Dyskinesia N/A N/A No information
Tay Sachs N/A N/A No information
Todd's Paralysis N/A N/A No information
Tourette Syndrome N/A N/A estimated 1-10 per 1,000 children have Tourette syndrome, Genetics Home Reference website
Transient Ischemic Attack N/A N/A No information
Transmissible mink encephalopathy (TME) N/A N/A No information
Traumatic Brain Injury N/A N/A 0.2% of population has an acquired brain injury in Australia 1998 (Australia’s Health 2004, AIHW)
Tremor N/A N/A No information
Tuberous sclerosis N/A N/A less than 1 in 10,000
Variant CJD N/A N/A No information
Viral meningitis N/A N/A No information
Wallenberg's Syndrome N/A N/A No information
Wernicke's encephalopathy N/A N/A No information
Wernicke-Korsakoff syndrome N/A N/A No information
Western equine encephalitis N/A N/A No information
Williams Syndrome N/A N/A estimated 1 per 7,500 - 20,000 people suffer from Williams syndrome, Genetics Home Reference website
Wilson's Disease N/A N/A approximately 1 per 30,000 people suffer from Wilson disease, Genetics Home Reference website
Zellweger Syndrome N/A N/A rare
Japanese encephalitis N/A N/A No information
Pneumococcal meningitis N/A N/A No information
Vertigo 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
Brain Damage-Induced Synesthesia 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
Brain Stem Glioma N/A N/A No information
Medulloblastoma N/A N/A No information
Oligodendroglioma N/A N/A No information
Cerebrovascular accident N/A N/A No information
Extradural hematoma N/A N/A No information
Familial Febrile Convulsions, 2 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
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
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
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
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
Mental retardation -- epilepsy, X-linked 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
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
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
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
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
Spinocerebellar ataxia, X-linked, 2 N/A N/A No information
Spinocerebellar ataxia, X-linked, 3 N/A N/A No information
Lymphedema, microcephaly and chorioretinopathy syndrome N/A N/A No information
Proximal tubulopathy -- diabetes mellitus -- cerebellar ataxia 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
Fungal meningitis N/A N/A No information
Leptomeningitis N/A N/A No information
Central sleep apnea N/A N/A No information
Hypomyelination, Global Cerebral 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
Subacute sclerosing leukoencephalitis 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
Amyotrophic lateral sclerosis N/A N/A 4-8 per 1000,000 people suffer from amyotrophic lateral sclerosis worldwide, Genetics Home Reference website
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
Infectious meningitis N/A N/A No information
Normal Pressure Hydrocephalus 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
Mental retardation, keratoconus, febrile seizures, and sinoatrial block N/A N/A No information
Ceroid lipofuscinosis, neuronal 8, northern epilepsy variant N/A N/A No information
Primary Lateral Sclerosis N/A N/A rare
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
Catamenial seizure N/A N/A No information
Anosognosia N/A N/A No information
Gelastic seizure N/A N/A No information
Atonic seizure 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
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
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
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
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
Autonomic seizure N/A N/A No information
Simple partial seizure N/A N/A No information
Sensory seizure N/A N/A No information
Partial seizure 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
Basilar artery insufficiency N/A N/A No information
Stroke-like dysarthria N/A N/A No information
Alcoholic cerebellar degeneration N/A N/A No information
Stroke-like aphasia N/A N/A No information
Drop attacks as seen in stroke N/A N/A No information
Uremic encephalopathy N/A N/A No information
Brain stem lesions 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-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
Charcot-Marie-Tooth disease with ptosis and parkinsonism 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
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 familial amyotrophic lateral sclerosis type 2 has been reported in only a few families, Genetics Home Reference website
Amyotrophic lateral sclerosis, familial type 3 N/A N/A No information
Amyotrophic lateral sclerosis, familial type 4 N/A N/A familial amyotrophic lateral sclerosis type 4 has been reported in only a few families, Genetics Home Reference website
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 familial amyotrophic lateral sclerosis type 4 has been reported in only a few families, Genetics Home Reference website
Amyotrophic lateral sclerosis, familial N/A N/A 10% of all cases of amyotrophic lateral sclerosis are familial, Genetics Home Reference website
Amyotrophic lateral sclerosis type 1 N/A N/A 3% of sporadic cases of amyotrophic lateral sclerosis are type 1, Genetics Home Reference website
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
Lymphocytic Choriomeningitis N/A N/A No information
Granulomatous amebic encephalitis N/A N/A No information
Naegleria N/A N/A No information
Fissures N/A N/A No information
Subarachnoid haemorrhage N/A N/A No information
Focal seizures N/A N/A No information
Generalized seizures N/A N/A No information
Post-vaccinial encephalitis 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 N/A N/A No information
Spinocerebellar ataxia 3 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
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
Mental retardation, X-linked -- craniofacial dysmorphology -- epilepsy -- ophthalmoplegia -- cerebellar 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
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
Brain infection 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
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, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity 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
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy N/A N/A No information
Dandy-Walker malformation postaxial polydactyly N/A N/A No information
Dandy-Walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy N/A N/A No information
Microcephaly -- seizures -- mental retardation -- heart disorders 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
Microcephaly -- sparse hair -- mental retardation -- seizures N/A N/A No information
Pachygyria -- mental retardation -- seizures 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
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
Microcephaly -- mesobrachyphalangy -- tracheoesophageal fistula syndrome N/A N/A No information
Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance N/A N/A No information
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate 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
Spinocerebellar Ataxia N/A N/A No information
Myoclonus epilepsy N/A N/A No information
Progressive muscular atrophy N/A N/A No information
Occipital Neuralgia N/A N/A No information
Primary amoebic meningoencephalitis N/A N/A No information
Mild Traumatic Brain Injury N/A N/A No information
Leukoencephalopathy N/A N/A No information
Listeriosis meningoencephalitis N/A N/A No information
Rasmussen encephalitis 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
Microcephaly -- microphthalmia -- ectrodactyly of lower limbs -- prognathism 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
Opisthotonos N/A N/A No information
Fontanel bulging N/A N/A No information
Argyria N/A N/A No information
Brudzinski's sign 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
Post-traumatic epilepsy 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
Primary amebic meningoencephalitis N/A N/A No information
Spinocerebellar ataxia, X-linked, 4 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
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
Hallervorden-Spatz disease N/A N/A rare
Hallervorden-Spatz Syndrome N/A N/A No information
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
Dystonia-Parkinsonism, Adult-Onset N/A N/A No information
Limbic encephalitis 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
Pontocerebellar hypoplasia with infantile spinal muscular atrophy N/A N/A No information
Spinal muscular atrophy -- Dandy-Walker complex -- cataracts 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 anesthesia deafness intellectual deficit N/A N/A No information
Corneal hypesthesia deafness intellectual deficit N/A N/A No information
Corneal dystrophy -- ichthyosis -- microcephaly -- mental retardation 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
Olivopontocerebellar Atrophy, Hereditary 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
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
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, 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
California encephalitis N/A N/A No information
Cerebellar degeneration N/A N/A No information
Cerebral sarcoma N/A N/A No information
Amyloidosis VI N/A N/A No information
Amyloidosis, cerebroarterial, hereditary, Italian type 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
Lissencephaly, type 1, isolated, without known genetic defects 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 approximately 1 per 40,000 people of Ashkenazi Jewish descent have Niemann-Pick disease type A, Genetics Home Reference website
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 approximately 1 per 150,000 people have Niemann-Pick disease type C, Genetics Home Reference website
Niemann-Pick disease, type B 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
Lissencephaly syndrome type 1 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
Atherosclerosis- deafness -- diabetes -- epilepsy -- nephropathy 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
Encephalophathy recurrent of childhood N/A N/A No information
Primary lateral sclerosis, adult 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
Seckel syndrome 4 N/A N/A No information
Seckel syndrome 1 N/A N/A No information
Seckel syndrome 2 N/A N/A No information
Seckel syndrome 3 N/A N/A No information
Seckel syndrome N/A N/A No information
Seckel-like syndrome, type Buebel N/A N/A No information
Seckel-like syndrome, Majoor-Krakauer type N/A N/A No information
Cerebellar degeneration, subacute N/A N/A No information
Lennox-Gastaut Syndrome N/A N/A No information
Wyburn-Mason Syndrome N/A N/A No information
Wyburn Mason's syndrome 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
Arthrogryposis -- epileptic seizures -- migrational brain disorder N/A N/A No information
Borjeson-Forssman-Lehmann Syndrome 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
Microcephaly syndactyly brachymesophalangy 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
Herpes simplex encephalitis N/A N/A No information
Cerebro-facio-thoracic dysplasia N/A N/A No information
Craniosynostosis Fontaine type N/A N/A No information
Cerebral abscess N/A N/A No information
Cerebellar abscess 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
Aging brain syndrome N/A N/A No information
Reye's 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
Encephalomyelitis N/A N/A No information
Spina bifida N/A N/A No information
Anencephaly and spina bifida X-linked N/A N/A No information
Meningocele N/A N/A No information
Lateral meningocele syndrome N/A N/A No information
Osteoporosis -- macrocephaly -- mental retardation -- blindness N/A N/A No information
Corpus callosum dysgenesis X-linked recessive 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 0.5% of people suffer from cerebral cavernous malformations worldwide, Genetics Home Reference website
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
Glycine encephalopathy, classical neonatal form N/A N/A No information
Glycine encephalopathy, classical neonatal late-onset form 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
Mitochondrial encephalomyopathy -- aminoacidopathy N/A N/A No information
Muscular dystrophy -- white matter spongiosis N/A N/A No information
Syringomyelia, medulla oblongata lesion N/A N/A No information
Variant Creutzfeldt-Jakob disease N/A N/A No information
Prion disease N/A N/A No information
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
Holoprosencephaly deletion 2p 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
Decreased cerebral perfusion N/A N/A No information
Decorticate posture N/A N/A No information
Decorticate posture in children 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
Pontoneocerebellar Hypoplasia N/A N/A No information
Microcephaly -- mental retardation -- spasticity -- epilepsy 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
Corpus callosum, agenesis of, blepharophimosis Robin type N/A N/A No information
Oculocerebral dysplasia N/A N/A No information
Diprosopia 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
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
Granulomatous amoebic encephalitis N/A N/A No information
Akinetic mutism 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
Microcephaly -- mental retardation -- retinopathy 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
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
Hypoplastic right heart -- microcephaly N/A N/A No information
Microcephaly -- pontocerebellar hypoplasia -- dyskinesia 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
Acute hemorrhagic leukoencephalitis N/A N/A No information
Cerebral ventricle neoplasm N/A N/A No information
Tay-Sachs disease -- adult onset N/A N/A No information
Tay Sachs Disease N/A N/A No information
Machado-Joseph Disease N/A N/A rare
Dentatorubral Pallidoluysian Atrophy N/A N/A No information
Lafora body disease 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
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
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
Tay-Sachs disease -- juvenile onset N/A N/A No information
Vascular malformations of the brain N/A N/A No information
Juvenile primary lateral sclerosis N/A N/A only a few cases of juvenile primary lateral sclerosis have been reported, Genetics Home Reference website
Refsum disease with increased pipecolic acidemia 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
Agammaglobulinemia, microcephaly, and severe dermatitis N/A N/A No information
Encephalopathy due to sulphite oxidase deficiency N/A N/A No information
Dandy-Walker malformation with mental retardation, basal ganglia disease, and seizures 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
Auditory perceptual disorder N/A N/A No information
Idiopathic basal ganglia calcification, childhood onset N/A N/A No information
Progressive cerebellocerebral atrophy N/A N/A No information
Infantile cerebellar atrophy 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
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
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
Glioma N/A N/A No information
Desmoplastic cerebral astrocytoma of infancy 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
Refsum disease, infantile form N/A N/A No information
Nipah virus encephalitis N/A N/A No information
Paraneoplastic limbic encephalitis N/A N/A No information
Ependymoma N/A N/A No information
Pineoblastoma, adult N/A N/A No information
Methylmalonic aciduria -- microcephaly -- cataract N/A N/A No information
Seizures -- intellectual deficit due to hydroxylysinuria 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
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
Canavan leukodystrophy 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
Rokitansky Van Bogaert syndrome N/A N/A No information
Nyssen-Van Bogaert syndrome N/A N/A No information
Hereditary ataxia 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
Ectodermal dysplasia -- mental retardation -- central nervous system malformation 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
Endocrine-Cerebroosteodysplasia N/A N/A No information
Cystic leukoencephalopathy without megalencephaly N/A N/A No information
Heterotopia, Periventricular, Associated with Chromosome 5q Deletion N/A N/A No information
Neurodegeneration With Brain Iron Accumulation 2 N/A N/A No information
Microcephaly-Faciocardioskeletal syndrome N/A N/A No information
Zechi-Ceide Syndrome N/A N/A No information
Frontotemporal dementia 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
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
Congenital brain dysgenesis due to glutamine synthetase deficiency N/A N/A No information
Microcephaly -- facial clefting -- preaxial polydactyly N/A N/A No information
Subependymoma 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
Corpus callosum dysgenesis cleft spasm N/A N/A No information
Cataract -- Hypertrichosis -- Intellectual Deficit N/A N/A No information
Arena synddrome N/A N/A No information
Encephalopathy due to GLUT1 deficiency 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
Microcephaly, primary autosomal recessive N/A N/A No information
Robinow-Unger syndrome 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
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
Neural tube defect, folate-sensitive N/A N/A No information
Craniosynostosis -- alopecia -- brain defect N/A N/A No information
Midline field defects 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
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
Cerebral Amyloid Angiopathy, Familial N/A N/A No information
Corpus callosum agenesis-neuropathy N/A N/A No information
Holoprosencephaly -- caudal dysgenesis N/A N/A No information
Kaufman oculocerebrofacial syndrome 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
Absent corpus callosum -- cataract -- immunodeficiency N/A N/A No information
X-linked hydrocephalus spectrum 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
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
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
Microcephaly -- glomerulonephritis -- Marfanoid habitus N/A N/A No information
Microcephalic primordial dwarfism, Toriello type N/A N/A No information
HARD syndrome 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
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
Obesity, hypothyroidism, craniosynostosis, cardial hypertrophy, colitis and intellectual deficiency 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
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
Muscle-eye-brain syndrome N/A N/A No information
Parenchymatous cortical degeneration of cerebellum N/A N/A No information
Intracranial arteriovenous malformation N/A N/A No information
Encephalopathy progressive -- optic atrophy 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
Nova syndrome N/A N/A No information
Meckel syndrome type 2 N/A N/A No information
Lysteria monocytoigeneses meningitis N/A N/A No information
Meckel Syndrome N/A N/A No information
Meckel syndrome type 3 N/A N/A No information
Meckel syndrome, type 5 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
Microcephalic osteodysplastic primordial dwarfism, type 2 N/A N/A No information
Microcephalic osteodysplastic primordial dwarfism, type 3 N/A N/A No information
Microcephaly -- microphthalmos -- blindness N/A N/A No information
Rasmussen subacute encephalitis 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
Hemimegalencephaly N/A N/A No information
Meningoencephalocele 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
Cerebellum agenesis -- hydrocephaly 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
Holoprosencephaly, recurrent infections, and monocytosis 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
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
$3C syndrome$ 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
Corpus callosum dysgenesis hypopituitarism N/A N/A No information
Agyria-pachygyria type 1 N/A N/A No information
Apallic syndrome 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
Oligodontia, microcephaly, short stature and characteristic facies N/A N/A No information
Fochs-LADD N/A N/A No information
Hypotonia -- failure to thrive -- microcephaly 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
Central pontine myelinolysis 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
Leigh syndrome, Saguenay-Lac-St. Jean type N/A N/A No information
Stevenson-Carey syndrome N/A N/A No information
Lymphoedema -- cerebral arteriovenous anomaly N/A N/A No information
Anton-Vogt syndrome N/A N/A No information
Limbic encephalitis -- neuromyotonia -- hyperhidrosis -- polyneuropathy N/A N/A No information
Shy-Drager Syndrome N/A N/A No information
Sturge-Weber Syndrome N/A N/A No information
Intracranial arachnoid cysts N/A N/A No information
Cadasil N/A N/A about 400 people have been diagnosed with CADASIL worldwide, Genetics Home Reference website
Gliosis N/A N/A No information
GSS N/A N/A No information
Neu-Laxova Syndrome N/A N/A No information
Moyamoya Syndrome N/A N/A No information
Walker-Warburg Syndrome N/A N/A No information
Osteopaenia -- myopia -- hearing loss -- intellectual deficit -- facial dysmorphism 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
Hyperkinetic dysarthria 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
Binswanger Disease N/A N/A No information
Cerebrorenodigital syndrome N/A N/A No information
Diencephalic Syndrome N/A N/A No information
Mulibrey Nanism 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
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
Revesz Debuse syndrome N/A N/A No information
Retinopathy -- anaemia- CNS anomalies N/A N/A No information
Revesz Syndrome 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
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 estimated 1-3 per 1 million people are affected by Hallervorden-Spatz disease worldwide, Genetics Home Reference website
PEHO-like syndrome N/A N/A No information
Saguenay-Lac Saint Jean -- COX deficiency N/A N/A No information
Bonnemann-Meinecke-Reich syndrome 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
Pick's disease of the brain N/A N/A No information
Cerebro-oculo-nasal 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
Strauss syndrome N/A N/A No information
ADANE 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
Heidenhain syndrome N/A N/A No information
Homen 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
Krause syndrome 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
May-White syndrome N/A N/A No information
Osuntokun 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
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
Double cortex syndrome N/A N/A No information
Basilar impression primary N/A N/A No information
Hordnes-Engebretsen-Knudtson syndrome 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
Chitayat-Moore-Del Bigio syndrome 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
Leukomalacia 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
Brun's syndrome N/A N/A No information
Bald soprano syndrome N/A N/A No information
Bartschi-Rochaix syndrome N/A N/A No information
Bessman-Baldwin syndrome N/A N/A No information
Borries syndrome N/A N/A No information
Brown-Symmers disease 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
MoyaMoya disease 1 N/A N/A No information
Hydrocephalus due to congenital stenosis of aqueduct of sylvius N/A N/A No information
Saal-Bulas syndrome N/A N/A No information
Micro syndrome N/A N/A No information
Southwestern Athabaskan genetic diseases 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
MoyaMoya disease 2 N/A N/A No information
MoyaMoya disease 3 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
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
Jung-Wolff-Back-Stahl syndrome N/A N/A No information
Microcephaly -- hypergonadotropic hypogonadism -- short stature N/A N/A No information
Plum syndrome N/A N/A No information
Neuroectodermal endocrine syndrome N/A N/A No information
Cerebro oculo skeleto renal 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
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
Facial asymetry -- temporal seizures N/A N/A No information
Dysplastic cortical hyperostosis N/A N/A No information
Kozlowski-Brown-Hardwick syndrome N/A N/A No information
Morse-Rawnsley-Sargent syndrome N/A N/A No information
Rambaud-Galian syndrome N/A N/A No information
COACH syndrome N/A N/A No information
HEC 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
Steinfeld syndrome N/A N/A No information
Cerebral gigantism -- jaw cysts N/A N/A No information
Susac syndrome N/A N/A No information
Dincsoy-Salih-Patel syndrome N/A N/A No information
Sengers-Hamel-Otten syndrome N/A N/A No information
Mowat-Wilson 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
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
Arakawa syndrome 1 N/A N/A No information
Angiomatosis, diffuse corticomeningeal, of Divry and Van Bogaert N/A N/A No information
Balo disease 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
Baker-Vinters 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
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
Craniotelencephalic dysplasia N/A N/A No information
Boucher-Neuhauser syndrome 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
Lafora disease N/A N/A No information
Nielsen-Jacobs syndrome N/A N/A No information
Severe achondroplasia with developmental delay and acanthosis nigricans N/A N/A only a few cases of SADDAN have been reported worldwide, Genetics Home Reference website
Delleman-Oorthuys syndrome N/A N/A No information
Marie type ataxia N/A N/A No information
Craniodiaphyseal dysplasia 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
Absence of septum pellucidum and septo-optic dysplasia 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
Worster Drought syndrome N/A N/A No information
Von voss Cherstvoy syndrome N/A N/A No information
Sabin-Feldman syndrome 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
Herrmann syndrome N/A N/A No information
Silverman-Handmaker syndrome N/A N/A No information
Limb-body wall complex N/A N/A No information
Encephalo cranio cutaneous lipomatosis 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
Balo's concentric sclerosis 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
Pelizaeus-Merzbacher disease, adult onset N/A N/A No information

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Types of Brain conditions

For more information about types of Brain conditions, refer to our section on types of Brain conditions. See also more information on death information for Brain conditions.

 

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