This section presents information about the death rate statistics
for the various types of Neuromuscular conditions.
Disease | Death Rate Estimate | US deaths 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 |
N/A |
N/A |
1 per 6,000 - 10,000 people suffer from spinal muscular atrophy, Genetics Home Reference website
|
| Spinal Muscular Atrophy type I |
N/A |
N/A |
No information
|
| Spinal Muscular Atrophy type II |
N/A |
N/A |
No information
|
| Spinal Muscular Atrophy type III |
N/A |
N/A |
No information
|
| 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 |
N/A |
N/A |
1 per 3,500 - 5,000 male newborns suffer from muscular dystrophy, Duchenne and Becker types, Genetics Home Reference website
|
| Adult progressive spinal muscular atrophy, Aran Duchenne type |
N/A |
N/A |
No information
|
| Becker's muscular dystrophy (BMD) |
N/A |
N/A |
No information
|
| Muscular dystrophy, limb-girdle, autosomal recessive, type 2K |
N/A |
N/A |
No information
|
| Muscular dystrophy, limb-girdle, autosomal dominant, type 1F |
N/A |
N/A |
No information
|
| Muscular dystrophy, limb-girdle, autosomal dominant, type 1G |
N/A |
N/A |
No information
|
| Muscular dystrophy, limb-girdle -- mental retardation |
N/A |
N/A |
No information
|
| Limb-girdle muscular dystrophy type 1B |
N/A |
N/A |
No information
|
| Limb-Girdle muscular dystrophy type 2A |
N/A |
N/A |
No information
|
| Limb-girdle muscular dystrophy type 1A |
N/A |
N/A |
No information
|
| Limb-girdle muscular dystrophy type 2B |
N/A |
N/A |
No information
|
| Limb-girdle muscular dystrophy type 1C |
N/A |
N/A |
No information
|
| Limb-girdle muscular dystrophy type 2C |
N/A |
N/A |
No information
|
| Limb-girdle muscular dystrophy type 1D |
N/A |
N/A |
No information
|
| Limb-girdle muscular dystrophy type 2D |
N/A |
N/A |
No information
|
| Limb-girdle muscular dystrophy type 1E |
N/A |
N/A |
No information
|
| Spinocerebellar ataxia 2 |
N/A |
N/A |
No information
|
| Limb-girdle muscular dystrophy type 2E |
N/A |
N/A |
No information
|
| Limb-girdle muscular dystrophy type 2F |
N/A |
N/A |
No information
|
| Spinocerebellar ataxia 4 |
N/A |
N/A |
No information
|
| Limb-girdle muscular dystrophy type 2G |
N/A |
N/A |
No information
|
| Spinocerebellar ataxia 5 |
N/A |
N/A |
No information
|
| Limb-girdle muscular dystrophy type 2H |
N/A |
N/A |
No information
|
| Limb-girdle muscular dystrophy type 2I |
N/A |
N/A |
No information
|
| Muscular dystrophy, limb girdle |
N/A |
N/A |
No information
|
| Muscular dystrophy, limb-girdle, autosomal dominant |
N/A |
N/A |
No information
|
| Spinocerebellar ataxia, Machado-Joseph type I |
N/A |
N/A |
No information
|
| Myopathy, limb-girdle, with bone fragility |
N/A |
N/A |
No information
|
| Muscular dystrophy, limb-girdle type 2M |
N/A |
N/A |
No information
|
| Muscular dystrophy limb girdle type 2A, Erb type |
N/A |
N/A |
No information
|
| Muscular dystrophy, limb-girdle, autosomal recessive, type 2H |
N/A |
N/A |
No information
|
| Muscular dystrophy, limb-girdle, autosomal recessive, type 2B |
N/A |
N/A |
No information
|
| Muscular dystrophy, limb girdle, autosomal recessive, type 2A |
N/A |
N/A |
No information
|
| Muscular dystrophy, limb-girdle, autosomal recessive, type 2E |
N/A |
N/A |
No information
|
| Myasthenia, Limb-Girdle, with Tubular Aggregates |
N/A |
N/A |
No information
|
| Muscular Dystrophy, Limb-Girdle, Type 3 |
N/A |
N/A |
No information
|
| Limb-girdle Muscular Dystropy type 1B |
N/A |
N/A |
No information
|
| Parkinson's disease dementia, familial |
N/A |
N/A |
No information
|
| Autosomal recessive limb-girdle muscular dystrophy, type 2G |
N/A |
N/A |
No information
|
| Muscular dystrophy limb-girdle (generic term) |
N/A |
N/A |
No information
|
| Primary Parkinsonism |
N/A |
N/A |
No information
|
| Genetic Parkinson disease |
N/A |
N/A |
No information
|
| Parkinson disease, genetic types |
N/A |
N/A |
No information
|
| Parkinson disease 4, autosomal dominant, Lewy body |
N/A |
N/A |
No information
|
| Parkinson disease 7, autosomal recessive, early-onset |
N/A |
N/A |
No information
|
| Dystonia musculorum deformans type 1 |
N/A |
N/A |
No information
|
| Spinocerebellar ataxia, X-linked, 2 |
N/A |
N/A |
No information
|
| Spastic paraplegia 2, X-linked |
N/A |
N/A |
No information
|
| Dystonia musculorum deformans type 2 |
N/A |
N/A |
No information
|
| Spinocerebellar ataxia, X-linked, 3 |
N/A |
N/A |
No information
|
| 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 |
1 million people (unreliable estimate) |
1 million people (unreliable estimate)
|
| Paralysis |
N/A |
N/A |
9 per 1000 - NHIS95 (paralysis of extremeties complete/partial)
|
| Paraplegia |
N/A |
N/A |
No information
|
| 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 |
N/A |
N/A |
4-8 per 1000,000 people suffer from amyotrophic lateral sclerosis worldwide, Genetics Home Reference website
|
| Myasthenia Gravis |
N/A |
N/A |
about 5 per 100,000 to 14 per 100,000 (NWHIC)
|
| Neonatal myasthenia |
N/A |
N/A |
No information
|
| Fibromyalgia |
N/A |
N/A |
3.7 million Americans (NIAMS)
|
| Tropical Spastic Paraparesis |
N/A |
N/A |
No information
|
| Guillain-Barre Syndrome |
N/A |
N/A |
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 |
N/A |
N/A |
150,000 people are affected by Charcot-Marie-Tooth disease in the US, Genetics Home Reference website
|
| Charcot disease |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease, Type 2K |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease with ptosis and parkinsonism |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth type 1 aplasia cutis congenital |
N/A |
N/A |
No information
|
| Torsion dystonia 7 |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease, Type 2B1 |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease, Type 2B2 |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease, Type 4B1 |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease, Type 4B2 |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease, Type 2AI |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease, dominant intermediate 1 |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease, dominant intermediate 2 |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease, dominant intermediate 3 |
N/A |
N/A |
No information
|
| Spastic paraplegia type 1, X-linked |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease deafness recessive type |
N/A |
N/A |
No information
|
| Charcot-Marie-Tooth disease, Type 2F |
N/A |
N/A |
No information
|
| Autosomal Dominant Charcot-Marie-Tooth with hearing loss |
N/A |
N/A |
No information
|
| Spastic Paraplegia 18, Autosomal Recessive |
N/A |
N/A |
No information
|
| Spastic paraplegia 11, autosomal recessive |
N/A |
N/A |
No information
|
| Spastic paraplegia 23 |
N/A |
N/A |
No information
|
| Spastic paraplegia 17 |
N/A |
N/A |
No information
|
| Spastic paraplegia 20, autosomal recessive |
N/A |
N/A |
No information
|
| Spastic paraplegia 14, autosomal recessive |
N/A |
N/A |
No information
|
| Spastic paraplegia 15, autosomal recessive |
N/A |
N/A |
No information
|
| Spastic paraplegia 25, autosomal recessive |
N/A |
N/A |
No information
|
| Spastic paraplegia 26, autosomal recessive |
N/A |
N/A |
No information
|
| Spastic paraplegia 16, X-linked |
N/A |
N/A |
No information
|
| Spastic paraplegia 10, autosomal dominant |
N/A |
N/A |
No information
|
| Spastic paraplegia 12, autosomal dominant |
N/A |
N/A |
No information
|
| Spastic paraplegia 13, autosomal dominant |
N/A |
N/A |
No information
|
| Spastic paraplegia 19, autosomal dominant |
N/A |
N/A |
No information
|
| Spastic paraplegia 29, autosomal dominant |
N/A |
N/A |
No information
|
| Spastic paraplegia 7, autosomal recessive |
N/A |
N/A |
No information
|
| Spastic paraplegia 39, autosomal recessive |
N/A |
N/A |
No information
|
| Spastic paraplegia 31, autosomal dominant |
N/A |
N/A |
No information
|
| Parkinsonism, early onset with mental retardation |
N/A |
N/A |
No information
|
| Cerebral Palsy |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis 7 |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis 8 |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis, 9 |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis 2, juvenile |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis 4, juvenile |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis, type 6 |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis, familial type 1 |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis, familial type 2 |
N/A |
N/A |
familial amyotrophic lateral sclerosis type 2 has been reported in only a few families, Genetics Home Reference website
|
| Amyotrophic lateral sclerosis, familial type 3 |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis, familial type 4 |
N/A |
N/A |
familial amyotrophic lateral sclerosis type 4 has been reported in only a few families, Genetics Home Reference website
|
| Amyotrophic lateral sclerosis, familial type 5 |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis, familial type 6 |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis, familial type 7 |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis, familial type 8 |
N/A |
N/A |
familial amyotrophic lateral sclerosis type 4 has been reported in only a few families, Genetics Home Reference website
|
| Amyotrophic lateral sclerosis, familial |
N/A |
N/A |
10% of all cases of amyotrophic lateral sclerosis are familial, Genetics Home Reference website
|
| Amyotrophic lateral sclerosis type 1 |
N/A |
N/A |
3% of sporadic cases of amyotrophic lateral sclerosis are type 1, Genetics Home Reference website
|
| Amyotrophic lateral sclerosis-parkinsonism/dementia complex 2 |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis-parkinsonism-dementia complex |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis 3 |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis 5 |
N/A |
N/A |
No information
|
| Amyotrophic lateral sclerosis 6 |
N/A |
N/A |
No information
|
| 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 |
N/A |
N/A |
estimated 1 per 40,000 people are affected by Friedreich ataxia, Genetics Home Reference website
|
| Spinal muscular atrophy, type 3 |
N/A |
N/A |
No information
|
| Spinal muscular atrophy with respiratory distress 1 |
N/A |
N/A |
No information
|
| Spinal muscular atrophy type 2 |
N/A |
N/A |
No information
|
| Spinal muscular atrophy, type I, with congenital bone fractures |
N/A |
N/A |
No information
|
| Spinal muscular atrophy, Ryukyuan type |
N/A |
N/A |
No information
|
| Athetoid Cerebral Palsy |
N/A |
N/A |
No information
|
| Mixed Cerebral Palsy |
N/A |
N/A |
No information
|
| Cerebral Palsy, Ataxic, Autosomal Recessive |
N/A |
N/A |
No information
|
| Cerebral Palsy, Spastic Quadriplegic, 1 |
N/A |
N/A |
No information
|
| Cerebral Palsy, Spastic Quadriplegic, 2 |
N/A |
N/A |
No information
|
| Cerebral Palsy, Spastic Quadriplegic, 3 |
N/A |
N/A |
No information
|
| 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 |
N/A |
N/A |
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 |
N/A |
N/A |
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 |
N/A |
N/A |
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 |
N/A |
N/A |
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 |
N/A |
N/A |
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
|
