| Disease | Prevalence Estimate | US people estimate | Statistic Used for Calculation |
| Cardiomyopathy -- hypotonia -- lactic acidosis |
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
|
| 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
|
| 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
|
| 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
|
| Fasciculations |
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
|
| Charcot-Marie-Tooth disease, X-linked, 1 |
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
|
| Opththalmoplegia |
N/A |
N/A |
No information
|
| Nemaline myopathy 1 |
N/A |
N/A |
No information
|
| Nemaline myopathy 2 |
N/A |
N/A |
No information
|
| Nemaline myopathy 3 |
N/A |
N/A |
No information
|
| Nemaline myopathy 4 |
N/A |
N/A |
No information
|
| Nemaline myopathy 5 |
N/A |
N/A |
No information
|
| Nemaline myopathy 6 |
N/A |
N/A |
No information
|
| Nemaline myopathy 7 |
N/A |
N/A |
No information
|
| Emery-Dreifuss Muscular Dystrophy 5 |
N/A |
N/A |
No information
|
| Emery-Dreifuss Muscular Dystrophy 4 |
N/A |
N/A |
No information
|
| Emery-Dreifuss Muscular Dystrophy 3 |
N/A |
N/A |
No information
|
| Emery-Dreifuss Muscular Dystrophy 2 |
N/A |
N/A |
No information
|
| Emery-Dreifuss Muscular Dystrophy 1 |
N/A |
N/A |
No information
|
| Emery-Dreifuss Syndrome |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis, 11 |
N/A |
N/A |
No information
|
| Hypoactive deep tendon reflexes |
N/A |
N/A |
No information
|
| Hyperreflexia |
N/A |
N/A |
No information
|
| Hyperreflexia in children |
N/A |
N/A |
No information
|
| Autosomal recessive spastic paraplegia, type 11 |
N/A |
N/A |
No information
|
| Decreased reflex response |
N/A |
N/A |
No information
|
| Decreased reflexes |
N/A |
N/A |
No information
|
| 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
|
| Ocular Myasthenia Gravis |
N/A |
N/A |
No information
|
| Myasthenia, Familial Infantile, 1 |
N/A |
N/A |
No information
|
| Myasthenia Gravis with Thymus Hyperplasia |
N/A |
N/A |
No information
|
| Myasthenia, Congenital, Refractory to Acetylcholinesterase Inhibitors |
N/A |
N/A |
No information
|
| Deposition diseases related fibromyalgia |
N/A |
N/A |
No information
|
| Tension myositis related fibromyalgia |
N/A |
N/A |
No information
|
| Sleep disturbance related fibromyalgia |
N/A |
N/A |
No information
|
| Major depressive disorder related fibromyalgia |
N/A |
N/A |
No information
|
| SLE related fibromyalgia |
N/A |
N/A |
No information
|
| Rheumatoid arthritis related fibromyalgia |
N/A |
N/A |
No information
|
| Epstein Barr virus related fibromyalgia |
N/A |
N/A |
No information
|
| Secondary Fibromyalgia |
N/A |
N/A |
No information
|
| Primary Fibromyalgia |
N/A |
N/A |
No information
|
| 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
|
| Fibromyalgia |
approx 1 in 73 or 1.36% or 3.7 million people in USA |
3,699,999 |
3.7 million Americans (NIAMS)
|
| Tropical Spastic Paraparesis |
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)
|
| Spastic paraparesis |
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
|
| Phosphoglycerate Kinase Deficiency |
N/A |
N/A |
No information
|
| Carnitine Deficiency Syndromes |
N/A |
N/A |
No information
|
| Carnitine Palmitoyl Transferase II Deficiency |
N/A |
N/A |
No information
|
| Carnitine Palmitoyl Transferase I Deficiency |
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
|
| Upper motor neuron lesions like hyperactive DTRs in the legs |
N/A |
N/A |
No information
|
| Extraocular muscle palsies |
N/A |
N/A |
No information
|
| Oculomotor palsy |
N/A |
N/A |
No information
|
| Gullian-Barre-like hyporeflexia |
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
|
| Glycogen storage disease type 2 |
N/A |
N/A |
No information
|
| Infantile parkinsonism |
N/A |
N/A |
No information
|
| Spinocerebellar ataxia 3 |
N/A |
N/A |
No information
|
| Congenital Muscular Dystrophy |
N/A |
N/A |
No information
|
| Parkinson disease, juvenile, autosomal recessive |
N/A |
N/A |
No information
|
| Spinal bulbar motor neuropathy |
N/A |
N/A |
No information
|
| Erb's dystrophy |
N/A |
N/A |
No information
|
| Mental retardation, X-linked -- hypotonia -- facial dysmorphism -- aggressive 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
|
| 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
|
| Dystonia 6, torsion |
N/A |
N/A |
No information
|
| Spinocerebellar ataxia, autosomal recessive 2 |
N/A |
N/A |
No information
|
| Mental retardation, X-linked -- hypotonia -- recurrent Infections |
N/A |
N/A |
No information
|
| Mental retardation -- hypotonia -- skin hyperpigmentation |
N/A |
N/A |
No information
|
| Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy |
N/A |
N/A |
No information
|
| Ophthalmoplegia, progressive external -- scoliosis |
N/A |
N/A |
No information
|
| Spastic paraplegia epilepsy mental retardation |
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
|
| Macrostomia -- preauricular tags -- external ophthalmoplegia |
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
|
| Fronto-temporal dementia and Parkinsonism linked to chromosome 17 (FTDP-17) |
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
|
| Myotonic Dystrophy |
N/A |
N/A |
Type I myotonic dystrophy accounts for 98% of all cases of myotonic dystrophy, Genetics Home Reference website
|
| Friedreich's ataxia |
N/A |
N/A |
No information
|
| Spinocerebellar Ataxia |
N/A |
N/A |
No information
|
| Progressive external ophthalmoplegia |
N/A |
N/A |
No information
|
| Alternating Hemiplegia |
N/A |
N/A |
rare
|
| Motor neuron diseases |
N/A |
N/A |
No information
|
| Dystonias |
N/A |
N/A |
No information
|
| Hereditary Spastic Paraplegia |
N/A |
N/A |
No information
|
| Progressive muscular atrophy |
N/A |
N/A |
No information
|
| 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
|
| Down's syndrome-like hypotonia |
N/A |
N/A |
No information
|
| Extraocular motor nerve palsies |
N/A |
N/A |
No information
|
| Chvostek's sign |
N/A |
N/A |
No information
|
| Opisthotonos |
N/A |
N/A |
No information
|
| Infantile onset spinocerebellar ataxia |
N/A |
N/A |
No information
|
| Juvenile-onset dystonia |
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 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
|
| 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
|
| Focal dystonia |
N/A |
N/A |
No information
|
| Muscle Hypertonia |
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
|
| Myotonic dystrophy type 3 |
N/A |
N/A |
No information
|
| Congenital myotonic dystrophy |
approx 1 in 20 or 5.00% or 13.6 million people in USA |
13,600,000 |
5 per 100 000 people suffer from myotonic dystrophy in the US
|
| Myotonic dystrophy, type 2 |
N/A |
N/A |
No information
|
| Proximal myotonic dystrophy |
N/A |
N/A |
No information
|
| Dystonia 4, Torsion, Autosomal Dominant |
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
|
| Wieacker-Wolff Syndrome |
N/A |
N/A |
No information
|
| Spastic paraplegia nephritis deafness |
N/A |
N/A |
No information
|
| Radioulnar synostosis mental retardation hypotonia |
N/A |
N/A |
No information
|
| Primary lateral sclerosis, adult |
N/A |
N/A |
No information
|
| Hereditary carnitine deficiency myopathy |
N/A |
N/A |
No information
|
| Neuronopathy, distal, autosomal recessive, 3 |
N/A |
N/A |
No information
|
| Dystonia with cerebellar atrophy |
N/A |
N/A |
No information
|
| Allan-Herndon-Dudley Syndrome |
N/A |
N/A |
No information
|
| Epidermolysa bullosa simplex and limb girdle muscular dystrophy |
N/A |
N/A |
No information
|
| Congenital ichthyosis, microcephalus, quadriplegia |
N/A |
N/A |
No information
|
| Arthrogryposis due to muscular dystrophy |
N/A |
N/A |
No information
|
| Arthrogryposis -- ophthalmoplegia -- retinopathy |
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
|
| Optic atrophy -- ophthalmoplegia -- ptosis -- deafness -- myopathy |
N/A |
N/A |
No information
|
| Optic atrophy opthalmoplegia ptosis deafness myopia |
N/A |
N/A |
No information
|
| Deafness, Conductive Stapedial, With Ear Malformation and Facial Palsy |
N/A |
N/A |
No information
|
| Hypotonia, Seizures and Precocious Puberty |
N/A |
N/A |
No information
|
| Congenital SMA with arthrogryposis |
N/A |
N/A |
rare
|
| Oculopharyngeal Muscular Dystrophy |
N/A |
N/A |
No information
|
| Emery-Dreifuss Muscular Dystrophy |
N/A |
N/A |
No information
|
| Friedreich ataxia -- congenital glaucoma |
N/A |
N/A |
No information
|
| Ophthalmoplegia |
N/A |
N/A |
No information
|
| Hereditary inclusion body myopathy -- joint contractures -- ophthalmoplegia |
N/A |
N/A |
No information
|
| Scapuloperoneal amyotrophy |
N/A |
N/A |
No information
|
| Amyotrophy, neurogenic scapuloperoneal, New England type |
N/A |
N/A |
No information
|
| Scapuloperoneal syndrome, neurogenic, Kaeser type |
N/A |
N/A |
No information
|
| Scapuloperoneal myopathy, MYH7-related |
N/A |
N/A |
No information
|
| Brody myopathy |
N/A |
N/A |
No information
|
| Myopathy -- ophthalmoplegia -- hypoacousia -- areflexia |
N/A |
N/A |
No information
|
| Myopathy congenital multicore with external ophthalmoplegia |
N/A |
N/A |
No information
|
| Minicore myopathy with external ophthalmoplegia |
N/A |
N/A |
No information
|
| Desmin related myopathy |
N/A |
N/A |
No information
|
| Hereditary carnitine deficiency syndrome, myopathic |
N/A |
N/A |
No information
|
| Nemaline myopathy |
N/A |
N/A |
No information
|
| Carnitine palmitoyl transferase II deficiency, myopathic |
N/A |
N/A |
No information
|
| Nemalin myopathy, late onset type |
N/A |
N/A |
No information
|
| Nemaline myopathy, early onset type |
N/A |
N/A |
No information
|
| Landouzy-Dejerine muscular dystrophy |
N/A |
N/A |
No information
|
| Fukuyama type muscular dystrophy |
N/A |
N/A |
No information
|
| Emery-Dreifuss muscular dystrophy, X-linked |
approx 1 in 100,000 or 0.00% or 2,720 people in USA |
2,720 |
estimated 1 per 100,000 people suffer from X-linked Emery-Dreifuss muscular dystrophy, Genetics Home Reference website
|
| Muscular dystrophy, proximal, autosomal dominant, late onset type |
N/A |
N/A |
No information
|
| Emery-Dreifuss muscular dystrophy, dominant type |
N/A |
N/A |
No information
|
| Facioscapulohumeral muscular dystrophy 1a |
N/A |
N/A |
No information
|
| Muscular dystrophy congenital, merosin negative |
N/A |
N/A |
No information
|
| Muscular dystrophy, congenital, infantile with cataract -- hypogonadism |
N/A |
N/A |
No information
|
| Muscular dystrophy, congenital, merosin-positive |
N/A |
N/A |
No information
|
| Muscular dystrophy -- white matter spongiosis |
N/A |
N/A |
No information
|
| Scleroatonic muscular dystrophy |
N/A |
N/A |
No information
|
| Ophthalmoplegic Muscular dystrophy |
N/A |
N/A |
No information
|
| Muscular Dystrophy -- Late Onset |
N/A |
N/A |
No information
|
| Hypotonic sclerotic muscular dystrophy |
N/A |
N/A |
No information
|
| Congenital muscular dystrophy syringomyelia |
N/A |
N/A |
No information
|
| Muscular dystrophy, congenital, type 1C |
N/A |
N/A |
No information
|
| Muscular dystrophy -- congenital infantile cataract -- hypogonadism |
N/A |
N/A |
No information
|
| Facioscapulohumeral Muscular Dystrophy -- Sensorineural Hearing Loss |
N/A |
N/A |
No information
|
| Muscular Dystrophy, Emery Dreifuss |
N/A |
N/A |
No information
|
| Muscular dystrophy congenital, with integrin deficiency |
N/A |
N/A |
No information
|
| Ceroid storage disease |
N/A |
N/A |
No information
|
| Decreased ankle and knee reflexes |
N/A |
N/A |
No information
|
| Nephronophthisis familial, adult -- spastic quadriparesis |
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
|
| Benign congenital hypotonia |
N/A |
N/A |
No information
|
| Paramyotonia congenita |
approx 1 in 100,000 or 0.00% or 2,720 people in USA |
2,720 |
less than 1 per 100,000 people are affected by paramyotonia congenital, 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
|
| Roussy-Levy hereditary areflexic dystasia |
N/A |
N/A |
No information
|
| Neuropathy, distal hereditary motor, Jerash type |
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
|
| Cerebral palsy, spastic, diplegic |
N/A |
N/A |
No information
|
| Machado-Joseph Disease |
N/A |
N/A |
rare
|
| Kearns-Sayre Syndrome |
N/A |
N/A |
rare
|
| 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
|
| Carnitine palmitoyl transferase deficiency |
N/A |
N/A |
No information
|
| Carnitine palmitoyl transferase 2 deficiency |
N/A |
N/A |
No information
|
| Spastic paraplegia glaucoma precocious puberty |
N/A |
N/A |
No information
|
| Hereditary carnitine deficiency |
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
|
| Muxcle Phosphoglycerate mutase deficiency |
N/A |
N/A |
No information
|
| Muscle phosphoglycerate kinase deficiency |
N/A |
N/A |
No information
|
| Carnitine palmitoyl transferase 1 deficiency |
approx 1 in 120,000,000 or 0.00% or 2 people in USA |
2 |
less than 50 people suffer from Jervell and Lange-Nielsen syndrome worldwide, Genetics Home Reference website
|
| Hereditary carnitine deficiency syndrome, systemic |
N/A |
N/A |
No information
|
| Carnitine palmitoyl transferase II deficiency, lethal neonatal form |
N/A |
N/A |
the lethal neonatal form of carnitine palitoyl transferase II deficiency has been reported in 10 families, Genetics Home Reference website
|
| Lactate dehydrogenase deficiency |
N/A |
N/A |
No information
|
| Hereditary carnitine deficiency syndrome |
N/A |
N/A |
No information
|
| Carnitine palmitoyl transferase II deficiency, infantile hepatocardiomuscular type |
N/A |
N/A |
the infantile hepatocardiomusucular form of carnitine palmitoyl transferase II deficiency has been reported in 10 families, Genetics Home Reference website
|
| Carnitine transporter deficiency |
approx 1 in 40,000 or 0.00% or 6,800 people in USA |
6,799 |
1 per 40,000 newborns suffer from primary carnitine deficiency in Japan, Genetics Home Reference website
|
| Phosphoglycerate kinase 1 deficiency |
N/A |
N/A |
No information
|
| Lactate dehydrogenase deficiency type A |
N/A |
N/A |
No information
|
| Lactate dehydrogenase deficiency type C |
N/A |
N/A |
No information
|
| Sixth nerve palsy, benign |
N/A |
N/A |
No information
|
| Hypotonia-cystinuria syndrome |
N/A |
N/A |
No information
|
| Cerebellar ataxia -- areflexia -- pes cavus -- optic atrophy -- sensorineural hearing loss |
N/A |
N/A |
No information
|
| Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss |
N/A |
N/A |
No information
|
| Developmental malformations -- deafness -- dystonia |
N/A |
N/A |
No information
|
| Oppenheim's dystonia |
N/A |
N/A |
No information
|
| Myasthenia, familial |
N/A |
N/A |
No information
|
| Idiopathic dystonia DYT1 |
N/A |
N/A |
No information
|
| Congenital myasthenic syndromes |
N/A |
N/A |
No information
|
| Paraplegia -- brachydactyly -- cone-shaped epiphysis |
N/A |
N/A |
No information
|
| Dystrophia myotonica 1 |
N/A |
N/A |
No information
|
| Spastic paraplegia with precocious puberty |
N/A |
N/A |
No information
|
| Spastic paraparesis deafness |
N/A |
N/A |
No information
|
| Lower motor neuron weakness |
N/A |
N/A |
No information
|
| Upper motor neuron weakness |
N/A |
N/A |
No information
|
| Neuropathy, distal hereditary motor |
N/A |
N/A |
No information
|
| Neuropathy, distal hereditary motor, type VIIA |
N/A |
N/A |
No information
|
| Polyradiculoneuropathy |
N/A |
N/A |
No information
|
| Neuropathy, distal hereditary motor, type III |
N/A |
N/A |
No information
|
| Congenital hypomyelination neuropathy |
N/A |
N/A |
No information
|
| Corpus callosum agenesis-neuropathy |
N/A |
N/A |
No information
|
| Giant axonal neuropathy |
N/A |
N/A |
No information
|
| Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis |
N/A |
N/A |
No information
|
| Myoclonic dystonia |
N/A |
N/A |
No information
|
| Infantile axonal neuropathy |
N/A |
N/A |
No information
|
| Spastic paraplegia -- neuropathy -- poikiloderma |
N/A |
N/A |
No information
|
| Facial paresis, hereditary, congenital |
N/A |
N/A |
No information
|
| Torsion dystonia, autosomal dominant |
N/A |
N/A |
No information
|
| Subacute Sclerosing Panencephalitis |
N/A |
N/A |
rare - because of the rarity of measles due to vaccination programs.
|
| Stiff-Person Syndrome |
N/A |
N/A |
rare
|
| Alternating hemiplegia of childhood |
N/A |
N/A |
No information
|
| Isaacs syndrome |
N/A |
N/A |
No information
|
| Spastic quadriplegia -- retinitis pigmentosa -- mental retardation |
N/A |
N/A |
No information
|
| Spinal atrophy -- ophthalmoplegia -- pyramidal syndrome |
N/A |
N/A |
No information
|
| 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
|
| Recurrent peripheral facial palsy |
N/A |
N/A |
No information
|
| Coarse face -- hypotonia -- constipation |
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
|
| Macrogyria, pseudobulbar palsy and mental retardation |
N/A |
N/A |
No information
|
| Neuritis with brachial predilection |
N/A |
N/A |
No information
|
| Neuronopathy, distal hereditary motor, type IIB |
N/A |
N/A |
No information
|
| Muscle Hypotonia |
N/A |
N/A |
No information
|
| Macrocephaly -- short stature -- paraplegia |
N/A |
N/A |
No information
|
| X-linked mental retardation -- hypotonia |
N/A |
N/A |
No information
|
| Opthalmoplegia ataxia hypoacusis |
N/A |
N/A |
No information
|
| Autonomic Dysreflexia |
N/A |
N/A |
No information
|
| Mc Leod neuroacanthocytosis syndrome |
N/A |
N/A |
No information
|
| Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency |
N/A |
N/A |
No information
|
| Unusual facies, hypotonia, mental retardation and radioulnar synostosis |
N/A |
N/A |
No information
|
| Monomelic Amyotrophy |
N/A |
N/A |
No information
|
| Neuromyotonia |
N/A |
N/A |
No information
|
| Locked-in Syndrome |
N/A |
N/A |
No information
|
| Polyneuropathy -- Ophthalmoplegia -- Leukoencehalopathy -- Intestinal Pseudo-Obstruction |
N/A |
N/A |
No information
|
| Spastic dysarthria |
N/A |
N/A |
No information
|
| Kuf Disease |
N/A |
N/A |
No information
|
| Ophtalmoplegia -- ataxia -- hypoacusis |
N/A |
N/A |
No information
|
| FOSMN 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
|
| Neuronal intranuclear inclusion disease |
N/A |
N/A |
No information
|
| Powell-Venencie-Gordon syndrome |
N/A |
N/A |
No information
|
| Lactate dehydrogenase deficiency type B |
N/A |
N/A |
No information
|
| Bahemuka Brown syndrome |
N/A |
N/A |
No information
|
| Perisylvian syndrome |
N/A |
N/A |
No information
|
| Sylvester (P.E.) syndrome |
N/A |
N/A |
No information
|
| Boucher-Neuhauser syndrome |
N/A |
N/A |
No information
|
| Seemanova-Lesny syndrome |
N/A |
N/A |
No information
|
| Becker disease |
N/A |
N/A |
No information
|
| Meige syndrome |
N/A |
N/A |
No information
|
| Ramsay Hunt Syndrome type I |
N/A |
N/A |
No information
|
| Parsonage Turner syndrome |
N/A |
N/A |
No information
|
| Worster Drought syndrome |
N/A |
N/A |
No information
|
| Wallerian degeneration |
N/A |
N/A |
No information
|
| Westphal disease |
N/A |
N/A |
No information
|
| Fazio-Londe syndrome |
N/A |
N/A |
No information
|
| King-Denborough syndrome |
N/A |
N/A |
No information
|
| Behr syndrome |
N/A |
N/A |
No information
|
| Ramsay Hunt syndrome Type II |
N/A |
N/A |
No information
|
The medical term 'prevalence' of Neuromuscular conditions usually refers to the estimated population
of people who are managing Neuromuscular conditions at any given time,
whereas the annual diagnosis rate of new cases of Neuromuscular conditions is called the 'incidence'.
For more information on prevalence and incidence statistics, see about prevalence and incidence statistics.
