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Diseases » Movement disorders » Deaths
 

Death Statistics for Types of Movement disorders

Deaths and Movement disorders:

This section presents information about the death rate statistics for the various types of Movement disorders.

Death Statistics for Types of Movement disorders

Disease

Death Rate Estimate

US deaths estimate

Statistic Used for Calculation

Familial Febrile Convulsions, 2 N/A N/A No information
Spastic Paraplegia 42, Autosomal Dominant 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
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
Tourette Syndrome N/A N/A estimated 1-10 per 1,000 children have Tourette syndrome, Genetics Home Reference website
Grand mal epilepsy N/A N/A No information
Spastic paraplegia 30, autosomal recessive N/A N/A No information
Spastic paraplegia 32, autosomal recessive 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
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
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
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 1 per 6,000 - 10,000 people suffer from spinal muscular atrophy, Genetics Home Reference website
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
Muscular Dystrophy N/A N/A No information
Duchenne Muscular Dystrophy N/A N/A No information
Becker Muscular Dystrophy N/A N/A No information
Limb-girdle Muscular Dystrophy N/A N/A No information
Muscular dystrophy, Duchenne and Becker type N/A N/A 1 per 3,500 - 5,000 male newborns suffer from muscular dystrophy, Duchenne and Becker types, Genetics Home Reference website
Adult progressive spinal muscular atrophy, Aran Duchenne type N/A N/A No information
Becker's muscular dystrophy (BMD) N/A N/A No information
Muscular dystrophy, limb-girdle, autosomal recessive, type 2K N/A N/A No information
Muscular dystrophy, limb-girdle, autosomal dominant, type 1F N/A N/A No information
Muscular dystrophy, limb-girdle, autosomal dominant, type 1G N/A N/A No information
Muscular dystrophy, limb-girdle -- mental retardation N/A N/A No information
Limb-girdle muscular dystrophy type 1B N/A N/A No information
Limb-Girdle muscular dystrophy type 2A N/A N/A No information
Limb-girdle muscular dystrophy type 1A N/A N/A No information
Limb-girdle muscular dystrophy type 2B N/A N/A No information
Limb-girdle muscular dystrophy type 1C N/A N/A No information
Limb-girdle muscular dystrophy type 2C N/A N/A No information
Limb-girdle muscular dystrophy type 1D N/A N/A No information
Limb-girdle muscular dystrophy type 2D N/A N/A No information
Limb-girdle muscular dystrophy type 1E N/A N/A No information
Spinocerebellar ataxia 2 N/A N/A No information
Limb-girdle muscular dystrophy type 2E N/A N/A No information
Limb-girdle muscular dystrophy type 2F N/A N/A No information
Spinocerebellar ataxia 4 N/A N/A No information
Limb-girdle muscular dystrophy type 2G N/A N/A No information
Spinocerebellar ataxia 5 N/A N/A No information
Limb-girdle muscular dystrophy type 2H N/A N/A No information
Limb-girdle muscular dystrophy type 2I N/A N/A No information
Muscular dystrophy, limb girdle N/A N/A No information
Muscular dystrophy, limb-girdle, autosomal dominant N/A N/A No information
Spinocerebellar ataxia, Machado-Joseph type I N/A N/A No information
Myopathy, limb-girdle, with bone fragility N/A N/A No information
Muscular dystrophy, limb-girdle type 2M N/A N/A No information
Muscular dystrophy limb girdle type 2A, Erb type N/A N/A No information
Muscular dystrophy, limb-girdle, autosomal recessive, type 2H N/A N/A No information
Muscular dystrophy, limb-girdle, autosomal recessive, type 2B N/A N/A No information
Muscular dystrophy, limb girdle, autosomal recessive, type 2A N/A N/A No information
Muscular dystrophy, limb-girdle, autosomal recessive, type 2E N/A N/A No information
Myasthenia, Limb-Girdle, with Tubular Aggregates N/A N/A No information
Muscular Dystrophy, Limb-Girdle, Type 3 N/A N/A No information
Limb-girdle Muscular Dystropy type 1B N/A N/A No information
Parkinson's disease dementia, familial N/A N/A No information
Autosomal recessive limb-girdle muscular dystrophy, type 2G N/A N/A No information
Muscular dystrophy limb-girdle (generic term) 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
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
Charcot-Marie-Tooth disease, X-linked, 1 N/A N/A No information
Proximal tubulopathy -- diabetes mellitus -- cerebellar ataxia 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
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
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
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
Bell's Palsy 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)
Paralysis N/A N/A 9 per 1000 - NHIS95 (paralysis of extremeties complete/partial)
Paraplegia N/A N/A No information
Convulsions N/A N/A No information
Opththalmoplegia 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
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
Autosomal recessive spastic paraplegia, type 11 N/A N/A No information
Decreased mobility N/A N/A No information
Decreased motion 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
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
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
Primary restless leg syndrome N/A N/A No information
Secondary restless leg syndrome N/A N/A No information
Muscle spasm N/A N/A No information
Contralateral athetosis 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
Myasthenia Gravis N/A N/A about 5 per 100,000 to 14 per 100,000 (NWHIC)
Neonatal myasthenia N/A N/A No information
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
Falls unavailable No information
Exercise N/A N/A No information
Guillain-Barre Syndrome N/A N/A about 1 in 100,000 (NWHIC)
Balo disease N/A N/A No information
Oculomotor Migraine N/A N/A No information
Spastic paraparesis N/A N/A No information
Multiple Sclerosis N/A N/A 1-in-700 (NIAID)
Myoclonus N/A N/A No information
Chorea N/A N/A No information
Sydenham chorea 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 rare
Progressive Supranuclear Palsy N/A N/A rare
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
Writer's cramp N/A N/A No information
Repetitive Strain Injury 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
Sixth nerve palsy N/A N/A No information
Paresis N/A N/A No information
Astasis N/A N/A No information
Focal motor seizure N/A N/A No information
Myoclonic seizures N/A N/A No information
Vestibular seizure N/A N/A No information
Hypnic jerk N/A N/A No information
Upper motor neuron lesions like hyperactive DTRs in the legs N/A N/A No information
Carpal spasm N/A N/A No information
Extraocular muscle palsies N/A N/A No information
Optic ataxia N/A N/A No information
Festinating gait N/A N/A No information
Spastic gait N/A N/A No information
Hemiballismus N/A N/A No information
Myopathic gait N/A N/A No information
Scissor gait N/A N/A No information
Choreoathetosis N/A N/A No information
Difficulty making fine hand movements N/A N/A No information
Sensory ataxia 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
Antalgic gait N/A N/A No information
Magnetic gait N/A N/A No information
Steepage gait N/A N/A No information
Limp in children N/A N/A No information
Rheumatic fever-like chorea N/A N/A No information
Cogwheel rigidity N/A N/A No information
Titubation 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
Charcot-Marie-Tooth disease -- deafness N/A N/A No information
Charcot-Marie-Tooth Disorder N/A N/A 150,000 people are affected by Charcot-Marie-Tooth disease in the US, Genetics Home Reference website
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
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
Parkinsonism, early onset with mental retardation N/A N/A No information
Cerebral Palsy 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
Tic disorders N/A N/A No information
Catalepsy N/A N/A No information
Catatonia N/A N/A No information
Delirium tremens N/A N/A No information
Akathisia N/A N/A No information
Recurring falls N/A N/A No information
Temporary paralysis N/A N/A No information
Occasional tremors N/A N/A No information
Pill rolling hand movements N/A N/A No information
Myoclonus epilepsy partial seizure N/A N/A No information
Infantile parkinsonism N/A N/A No information
Spinocerebellar ataxia 3 N/A N/A No information
Mobius syndrome N/A N/A rare
Parkinson disease, juvenile, autosomal recessive N/A N/A No information
Spinal bulbar motor neuropathy 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
Proximal spinal muscular atrophy, type 3 N/A N/A No information
Multiple system atrophy N/A N/A No information
Nystagmus, myoclonic 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
Ocular Muscular Dystrophy N/A N/A No information
Deafness conductive stapedial ear malformation facial palsy 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
Tics N/A N/A No information
Dystonia 6, torsion N/A N/A No information
Spinocerebellar ataxia, autosomal recessive 2 N/A N/A No information
Aniridia cerebellar ataxia mental deficiency N/A N/A No information
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy N/A N/A No information
Deafness hyperuricemia neurologic ataxia N/A N/A No information
Ataxia-oculomotor apraxia syndrome N/A N/A No information
Spastic paraplegia epilepsy mental retardation 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
Mental retardation, X-linked -- dystonia -- dysarthria N/A N/A No information
Ataxia-deafness syndrome N/A N/A No information
Ataxia, Hereditary, Autosomal Dominant N/A N/A No information
Ataxia spastic congenital miosis N/A N/A No information
Ataxia tapetoretinal degeneration N/A N/A No information
Ataxia with Vitamin E Deficiency N/A N/A No information
Athetosis N/A N/A No information
Iris dysplasia with ocular hypertelorism, psychomotor retardation and sensorineural deafness 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
Ataxia, spastic, 3, autosomal recessive N/A N/A No information
Fronto-temporal dementia and Parkinsonism linked to chromosome 17 (FTDP-17) 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
Idiopathic facial palsy 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
Myoclonus epilepsy N/A N/A No information
Alternating Hemiplegia N/A N/A rare
Motor neuron diseases N/A N/A No information
Dystonias N/A N/A No information
Hemifacial Spasm N/A N/A No information
Hereditary Spastic Paraplegia N/A N/A No information
Progressive muscular atrophy N/A N/A No information
Opsoclonus Myoclonus N/A N/A No information
Quadriplegia N/A N/A No information
Torsion dystonia, X-linked 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 estimated 1 per 40,000 people are affected by Friedreich ataxia, Genetics Home Reference website
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 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
Epilepsy-like myoclonic jerks N/A N/A No information
Extraocular motor nerve palsies N/A N/A No information
Brudzinski's sign N/A N/A No information
Infantile onset spinocerebellar ataxia N/A N/A No information
Juvenile-onset dystonia N/A N/A No information
Chorea familial benign N/A N/A No information
Bradykinesia 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
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
Dystonia-Parkinsonism, Adult-Onset N/A N/A No information
Torsion dystonia, autosomal recessive 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
Rett-like syndrome N/A N/A No information
Epilepsy with myoclonic-astatic crisis N/A N/A No information
Myokymia with neonatal epilepsy 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
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
Generalized epilepsy and paroxysmal dyskinesia N/A N/A No information
Hemiconvulsion-Hemiplegia-Epilepsy syndrome N/A N/A No information
Epilepsy, progressive myoclonic 3 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
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
Dystonia 4, Torsion, Autosomal Dominant N/A N/A No information
Choreoathetosis-spasticity, episodic N/A N/A No information
Motor neuropathy, peripheral with dysautonomia N/A N/A No information
Neuropathy -- ataxia -- retinitis pigmentosa N/A N/A No information
Multifocal motor neuropathy with conduction block N/A N/A No information
Neuropathy ataxia and retinis pigmentosa N/A N/A No information
Opthalmoplegia -- mental retardation -- lingua scrotalis 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
Ataxia N/A N/A No information
Bird-headed dwarfism with progressive ataxia, Insulin-resistant diabetes, goiter and primary gonadal insufficiency 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
Renal tubulopathy -- diabetes mellitus -- cerebellar ataxia N/A N/A No information
Ataxia -- diabetes -- goiter -- gonadal insufficiency 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
Primary lateral sclerosis, adult N/A N/A No information
Neuronopathy, distal, autosomal recessive, 3 N/A N/A No information
Episodic ataxia, type 7 N/A N/A No information
Episodic ataxia syndrome N/A N/A No information
Episodic ataxia, type 1 N/A N/A No information
Episodic ataxia, type 2 N/A N/A No information
Episodic ataxia, type 3 N/A N/A No information
Episodic ataxia, type 4 N/A N/A No information
Episodic ataxia, type 5 N/A N/A No information
Episodic ataxia, type 6 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
Congenital ichthyosis, microcephalus, quadriplegia 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
Camurati Engelmann disease, type 2 N/A N/A No information
Camurat-Engelmann disease, type 2 N/A N/A No information
Camurati-Engelmann Disease N/A N/A No information
Optic atrophy opthalmoplegia ptosis deafness myopia N/A N/A No information
Psychogenic Movement Disorders N/A N/A No information
Deafness, Conductive Stapedial, With Ear Malformation and Facial Palsy N/A N/A No information
Ataxia -- hypogonadism -- choroidal dystrophy N/A N/A No information
Duane Syndrome N/A N/A No information
Duane-radial ray syndrome N/A N/A only a few cases of Duane-radial ray syndrome have been reported, Genetics Home Reference website
Duane retraction syndrome II N/A N/A No information
Duane anomaly -- mental retardation N/A N/A No information
Duane retraction syndrome 2 N/A N/A No information
Duane retraction syndrome IC N/A N/A No information
Duane retraction syndrome IIA N/A N/A No information
Duane retraction syndrome IIB N/A N/A No information
Duane retraction syndrome IIC N/A N/A No information
Duane retraction syndrome III N/A N/A No information
Duane retraction syndrome I N/A N/A No information
Duane retraction syndrome IIIA N/A N/A No information
Duane retraction syndrome IIIB N/A N/A No information
Duane retraction syndrome IA N/A N/A No information
Duane retraction syndrome IIIC N/A N/A No information
Duane retraction syndrome IB N/A N/A No information
Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance N/A N/A No information
Sjogren-Larsson syndrome N/A N/A No information
Congenital SMA with arthrogryposis N/A N/A rare
Whispering dysphonia, hereditary N/A N/A No information
Ectodermal dysplasia -- hypohidrotic -- hypothyroidism -- ciliary dyskinesia N/A N/A No information
Nystagmus 1, congenital, X- linked N/A N/A No information
Nystagmus, congenital motor, autosomal recessive N/A N/A No information
Nystagmus 2, congenital, autosomal dominant N/A N/A No information
Nystagmus 3, congenital, autosomal dominant N/A N/A No information
Nystagmus 4, congenital, autosomal dominant N/A N/A No information
Nystagmus, congenital motor N/A N/A No information
Nystagmus, idiopathic congenital N/A N/A No information
Friedreich ataxia -- congenital glaucoma N/A N/A No information
Ataxia, spastic with congenital miosis N/A N/A No information
Ataxia with fasciculations N/A N/A No information
Brody myopathy N/A N/A No information
Primary orthostatic tremor N/A N/A No information
Ceroid storage disease 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
Microcephaly -- mental retardation -- spasticity -- epilepsy N/A N/A No information
Limb dystonia N/A N/A No information
Torsion dystonia with onset in infancy 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
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
Infantile striato-thalamic degeneration 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
Brachydactyly nystagmus cerebellar ataxia 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
Spastic tetraplegic -- cerebral palsy N/A N/A No information
Precocious myoclonic encephalopathy N/A N/A No information
Microcephaly -- pontocerebellar hypoplasia -- dyskinesia N/A N/A No information
Ocular motility disorders N/A N/A No information
Cerebral palsy, spastic, diplegic N/A N/A No information
Chorea, remitting with nystagmus and cataracts N/A N/A No information
Familial periodic paralysis 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
Machado-Joseph Disease N/A N/A rare
Dentatorubral Pallidoluysian Atrophy 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
Benign essential blepharospasm N/A N/A No information
Erb's Palsy 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
Cerebellar ataxia, infantile with progressive external ophthalmoplegia N/A N/A No information
Spastic paraplegia glaucoma precocious puberty N/A N/A No information
Torsion dystonia 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
Infantile Refsum Disease N/A N/A No information
ARCA N/A N/A No information
Fetal akinesia syndrome, X-linked N/A N/A No information
Hypobetalipoproteinaemia -- ataxia -- hearing loss N/A N/A No information
Gluten ataxia N/A N/A No information
Sarcoglycanopathy 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
Sixth nerve palsy, benign N/A N/A No information
Refsum disease, infantile form N/A N/A No information
Benign essential tremor syndrome N/A N/A No information
Dyskinesia, paroxysmal N/A N/A No information
Delta-sarcoglycanopathy N/A N/A No information
Anaemia, sideroblastic, X-linked -- ataxia N/A N/A No information
Neuroacanthocytosis 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
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
Anemia, sideroblastic spinocerebellar ataxia N/A N/A No information
Myoclonus, cerebellar ataxia, deafness N/A N/A No information
Leukodystrophy with oligodontia N/A N/A No information
Hereditary ataxia N/A N/A No information
Nephronophtisis familial, adult form -- spastic quadriparesia N/A N/A No information
Developmental malformations -- deafness -- dystonia N/A N/A No information
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa and Cataract N/A N/A No information
East Syndrome N/A N/A No information
Oppenheim's dystonia N/A N/A No information
Disseminated Sclerosis with Narcolepsy N/A N/A No information
Motor and cognitive disorder due to sepiapterin reductase deficiency N/A N/A No information
Hereditary paroxysmal cerebral ataxia N/A N/A No information
Myasthenia, familial N/A N/A No information
Idiopathic dystonia DYT1 N/A N/A No information
Unverricht-Lundborg disease N/A N/A No information
Unverricht-Lundborg syndrome N/A N/A No information
Corpus callosum dysgenesis cleft spasm N/A N/A No information
Ataxia, episodic -- vertigo -- tinnitus -- myokymia N/A N/A No information
Spinal shock N/A N/A No information
Lundberg I N/A N/A No information
Paraplegia -- brachydactyly -- cone-shaped epiphysis N/A N/A No information
Polydactyly cleft lip palate psychomotor retardation N/A N/A No information
Spastic paraplegia with precocious puberty N/A N/A No information
Distal hereditary motor neuropathy, type V N/A N/A only a few cases of distal hereditary motor neuropathy, type V have been reported, Genetics Home Reference website
Lower motor neuron weakness N/A N/A No information
Upper motor neuron weakness 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
Spastic paraplegia -- neuropathy -- poikiloderma N/A N/A No information
Facial paresis, hereditary, congenital N/A N/A No information
Idiopathic double athetosis 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
Ataxia -- oculomotor apraxia, type 1 N/A N/A No information
Apraxia, oculomotor, Cogan type N/A N/A No information
Corneal cerebellar syndrome N/A N/A No information
Corticobasal Degeneration N/A N/A No information
Infantile Spasms N/A N/A No information
Melkersson-Rosenthal Syndrome N/A N/A No information
Subacute Sclerosing Panencephalitis N/A N/A rare - because of the rarity of measles due to vaccination programs.
Tardive Dyskinesia N/A N/A No information
Cerebelloparenchymal disorder V N/A N/A No information
De Barsy Syndrome N/A N/A No information
Normokalemic periodic paralysis N/A N/A No information
Alternating hemiplegia of childhood N/A N/A No information
Spastic quadriplegia -- retinitis pigmentosa -- mental retardation 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
Opthalmoplegia -- myalgia -- tubular aggregates 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
Myoclonus-ataxia N/A N/A No information
Spastic paresis -- glaucoma -- mental retardation N/A N/A No information
Spastic paraplegia with Kallmann syndrome N/A N/A No information
Tsao-Ellingson syndrome N/A N/A No information
Aniridia -- renal agenesis -- psychomotor retardation 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
Bd syndrome N/A N/A No information
Arachnodactyly -- ataxia -- cataract -- aminoaciduria -- mental retardation N/A N/A No information
Quadrupedal gait, primitive speech and severe mental retardation 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
Alopecia -- hypogonadism -- extrapyramidal disorder N/A N/A No information
Degenerative motor system disease N/A N/A No information
Macrocephaly -- short stature -- paraplegia N/A N/A No information
Opthalmoplegia ataxia hypoacusis N/A N/A No information
Adversive syndrome N/A N/A No information
Hyperkinesis N/A N/A No information
Ossification anomalies -- psychomotor development N/A N/A No information
Anton-Vogt syndrome N/A N/A No information
Shy-Drager 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
Wernicke's encephalopathy N/A N/A No information
Benign Fasciculation Syndrome N/A N/A No information
Myokymia N/A N/A No information
Locked-in Syndrome N/A N/A No information
Sensorineural hearing loss, early greying, and essential tremor N/A N/A No information
Congenital Bilateral Perisylvian Syndrome N/A N/A No information
Kuf Disease N/A N/A No information
Ophtalmoplegia -- ataxia -- hypoacusis N/A N/A No information
Angelman-Like Syndrome, X-linked N/A N/A No information
Aniridia ataxia renal agenesis psychomotor retardation N/A N/A No information
Moebius sequence N/A N/A No information
Moebius syndrome 1 N/A N/A No information
Borud Syndrome N/A N/A No information
Cutler Syndrome N/A N/A No information
Moebius 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
Dancing Eye syndrome N/A N/A No information
Cirrhosis-like flapping tremens N/A N/A No information
Gustavson syndrome N/A N/A No information
Segawa syndrome, autosomal dominant N/A N/A No information
Segawa syndrome, autosomal recessive N/A N/A No information
Segawa Syndrome N/A N/A No information
Todd paralysis N/A N/A No information
Stiff baby syndrome N/A N/A No information
May-White syndrome N/A N/A No information
CACH syndrome N/A N/A No information
Apraxia, Ideomotor N/A N/A No information
Combarros Calleja Leno syndrome N/A N/A No information
Jankovic-Rivera syndrome N/A N/A No information
Conorenal Syndrome N/A N/A No information
Cramp-fasciculations syndrome N/A N/A No information
Choreoacanthocytosis amyotrophic N/A N/A No information
Bianchi's syndrome N/A N/A No information
Fanconi-Turler syndrome N/A N/A No information
Gamstorp-Wohlfart syndrome N/A N/A No information
Paroxysmal kinesigenic choreoathetosis N/A N/A No information
Myoclonus hereditary -- progressive distal muscular atrophy N/A N/A No information
Hyde-Forster-Mccarthy-Berry syndrome N/A N/A No information
Reardon-Wilson-Cavanagh syndrome N/A N/A No information
Supranuclear ocular palsy N/A N/A No information
Fitzsimmons-Walson-Mellor syndrome N/A N/A No information
Tome-Brune-Fardeau syndrome N/A N/A No information
ARTS syndrome N/A N/A No information
Richards-Rundle syndrome N/A N/A No information
Mousa-Al Din-Al Nassar syndrome N/A N/A No information
Pseudoprogeria syndrome N/A N/A No information
Powell-Venencie-Gordon syndrome N/A N/A No information
Dysequilibrium syndrome N/A N/A No information
Thomas-Jewett-Raines syndrome N/A N/A No information
Snyder-Robinson syndrome 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
Morse-Rawnsley-Sargent syndrome N/A N/A No information
COACH syndrome 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
Furukawa-Takagi-Nakao syndrome N/A N/A No information
Neuhauser-Daly-Magnelli syndrome N/A N/A No information
Schimke, X-linked, mental retardation syndrome N/A N/A No information
Fitzsimmons-McLachlan-Gilbert syndrome N/A N/A No information
Spastic ataxia, Charlevoix-Saguenay type N/A N/A No information
PANDAS N/A N/A No information
Pallidopyramidal syndrome N/A N/A No information
Dejerine-Klumpke syndrome N/A N/A No information
Mount Reback syndrome N/A N/A No information
Ziehen-Oppenheim 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
Geniospasm N/A N/A No information
Bangstad syndrome 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
Diomedi-Bernardi-Placidi syndrome N/A N/A No information
Fenton-Wilkinson-Toselano syndrome N/A N/A No information
Saul-Wilkes-Stevenson syndrome N/A N/A No information
Jeune-Tommasi syndrome N/A N/A No information
Boucher-Neuhauser syndrome N/A N/A No information
Gomez and Lopez-Hernandez syndrome N/A N/A No information
Paine syndrome N/A N/A No information
Marsden syndrome N/A N/A No information
Erythrokeratodermia ataxia N/A N/A No information
Becker disease N/A N/A No information
Marie type ataxia N/A N/A No information
Brown 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
Worster Drought syndrome N/A N/A No information
Westphal disease N/A N/A No information
Wells Jankovic syndrome N/A N/A No information
Oculomelic amyoplasia N/A N/A No information
Westphal-Leyden ataxia N/A N/A No information
Fazio-Londe syndrome N/A N/A No information
Hecht syndrome N/A N/A No information
Bobble-head doll syndrome N/A N/A No information
Behr syndrome N/A N/A No information
Riley Shwachman syndrome N/A N/A No information

Types of Movement disorders

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

 

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