| Disease | Prevalence Estimate | US people 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 |
approx 1 in 1,000 or 0.10% or 272,000 people in USA |
272,000 |
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 |
approx 1 in 6,000 or 0.02% or 45,333 people in USA |
45,333 |
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 |
approx 1 in 3,500 or 0.03% or 77,714 people in USA |
77,714 |
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 |
999,999 |
1 million people (unreliable estimate)
|
| Paralysis |
approx 1 in 111 or 0.90% or 2.4 million people in USA |
2,447,999 |
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 |
approx 1 in 250,000 or 0.00% or 1,087 people in USA |
5,000 |
4-8 per 1000,000 people suffer from amyotrophic lateral sclerosis worldwide, Genetics Home Reference website
|
| Myasthenia Gravis |
approx 1 in 20,000 or 0.00% or 13,600 people in USA |
13,599 |
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 |
N/A |
N/A |
No information
|
| Exercise |
N/A |
N/A |
No information
|
| Guillain-Barre Syndrome |
approx 1 in 100,000 or 0.00% or 2,720 people in USA |
2,720 |
about 1 in 100,000 (NWHIC)
|
| Balo disease |
N/A |
N/A |
No information
|
| Oculomotor Migraine |
N/A |
N/A |
No information
|
| Spastic paraparesis |
N/A |
N/A |
No information
|
| Multiple Sclerosis |
approx 1 in 700 or 0.14% or 388,571 people in USA |
388,571 |
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 |
approx 1 in 1,813 or 0.06% or 150,000 people in USA |
150,000 |
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 |
approx 1 in 10 or 10.00% or 27.2 million people in USA |
27,200,000 |
10% of all cases of amyotrophic lateral sclerosis are familial, Genetics Home Reference website
|
| Amyotrophic lateral sclerosis type 1 |
approx 1 in 33 or 3.00% or 8.2 million people in USA |
8,160,000 |
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 |
approx 1 in 40,000 or 0.00% or 6,800 people in USA |
6,799 |
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 |
approx 1 in 40,000 or 0.00% or 6,800 people in USA |
6,799 |
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 |
approx 1 in 12,000 or 0.01% or 22,666 people in USA |
22,666 |
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 |
approx 1 in 33,333 or 0.00% or 8,160 people in USA |
8,160 |
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 |
approx 1 in 10,000 or 0.01% or 27,200 people in USA |
27,199 |
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 |
approx 1 in 1,000,000 or 0.00% or 271 people in USA |
271 |
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
|
The medical term 'prevalence' of Movement disorders usually refers to the estimated population
of people who are managing Movement disorders at any given time,
whereas the annual diagnosis rate of new cases of Movement disorders is called the 'incidence'.
For more information on prevalence and incidence statistics, see about prevalence and incidence statistics.
