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Diseases » Muscle conditions » Incidence
 

Incidence Statistics for Types of Muscle conditions

The information below shows a list of types of Muscle conditions, with information as to the annual incidence of each of these types of Muscle conditions. Estimates of the people affected each year are calculated based on the available statistics.

Incidence Statistics for Types of Muscle conditions

Disease

Incidence Estimate

US people estimate

Statistic Used for Calculation

Muscle pain N/A N/A No information
Muscle weakness N/A N/A No information
Convulsions N/A N/A No information
Dermatomyositis N/A N/A No information
Febrile Seizures N/A N/A No information
Infantile Refsum Disease N/A N/A No information
Myasthenia Gravis N/A N/A No information
Myotonic Dystrophy N/A N/A No information
Open Wound approx 1 in 75 or 1.32% or 3.6 million people in USA 3,581,927 60,052 annual cases of open wounds in Victoria 1996 (DHS-VIC)
Progressive Spinobulbar muscular atrophy N/A N/A No information
Refsum Disease N/A N/A No information
Sarcoma N/A N/A No information
Soft Tissue Sarcoma approx 1 in 32,771 or 0.00% or 8,300 people in USA 8,299 8,300 annual cases (SEER 2002 estimate)
Myosarcoma N/A N/A No information
Rhabdomyosarcoma, embryonal N/A N/A No information
Rhabdomyosarcoma, alveolar N/A N/A No information
Leiomyosarcoma N/A N/A No information
Cardiomyopathy -- hypotonia -- lactic acidosis N/A N/A No information
Cardiomyopathy -- renal anomalies N/A N/A No information
Familial Febrile Convulsions, 2 N/A N/A No information
Spastic Paraplegia 42, Autosomal Dominant N/A N/A No information
Facioplegic migraine N/A N/A No information
Muscle contraction headache 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 hypertrophic cardiomyopathy 1 N/A N/A No information
Familial hypertrophic cardiomyopathy 2 N/A N/A No information
Familial hypertrophic cardiomyopathy 3 N/A N/A No information
Familial hypertrophic cardiomyopathy 4 N/A N/A No information
Familial hypertrophic cardiomyopathy 6 N/A N/A No information
Familial hypertrophic cardiomyopathy 7 N/A N/A No information
Familial hypertrophic cardiomyopathy 8 N/A N/A No information
Familial hypertrophic cardiomyopathy 9 N/A N/A No information
Familial hypertrophic cardiomyopathy 10 N/A N/A No information
Cardiomyopathy dilated 1B N/A N/A No information
Cardiomyopathy dilated 1C N/A N/A No information
Cardiomyopathy dilated 1D N/A N/A No information
Cardiomyopathy dilated 1E N/A N/A No information
Cardiomyopathy dilated 1G N/A N/A No information
Cardiomyopathy dilated 1H N/A N/A No information
Cardiomyopathy dilated 1I N/A N/A No information
Cardiomyopathy dilated 1J N/A N/A No information
Cardiomyopathy dilated 1K N/A N/A No information
Cardiomyopathy dilated 1L N/A N/A No information
Cardiomyopathy dilated 1M N/A N/A No information
Cardiomyopathy dilated 1P N/A N/A No information
Cardiomyopathy dilated 1Q N/A N/A No information
Cardiomyopathy dilated 1S N/A N/A No information
Cardiomyopathy dilated 1T N/A N/A No information
Cardiomyopathy dilated 1U N/A N/A No information
Cardiomyopathy dilated 1W N/A N/A No information
Cardiomyopathy dilated with conduction defect N/A N/A No information
Cardiomyopathy, Alcoholic N/A N/A No information
Cardiomyopathy diabetes deafness N/A N/A No information
Cardiomyopathy dilated 10 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
Grand mal seizures N/A N/A No information
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
Charcot-Marie-Tooth disease, X-linked recessive, 3 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
Kennedy Syndrome N/A N/A No information
Spinal Muscular Atrophy N/A N/A No information
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 approx 1 in 544,000 or 0.00% or 500 people in USA 500 500 - 600 male newborns are diagnosed with muscular dystrophy each year in the US, Duchenne and Becker types, Genetics Home Reference website
Duchenne Muscular Dystrophy approx 1 in 6,000 or 0.02% or 45,333 people in USA 45,333 about 1 in 3000 males1.
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 No information
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
Myasthenia, familial 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
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 approx 1 in 6,800 or 0.01% or 40,000 people in USA 40,000 40,000 annual cases in Americans
Parkinson's Disease N/A N/A No information
Paralysis N/A N/A No information
Paraplegia N/A N/A No information
Separated Rectus Abdominal Muscles N/A N/A No information
Cardiomyopathy N/A N/A No information
Dilated cardiomyopathy N/A N/A No information
Hypertrophic cardiomyopathy N/A N/A No information
Restrictive cardiomyopathy 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
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
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
Convulsions, benign familial infantile, 3 N/A N/A No information
Convulsions, benign familial infantile, 4 N/A N/A No information
Fromont Anomaly N/A N/A No information
Familial hypertrophic cardiomyopathy 12 N/A N/A No information
Familial hypertrophic cardiomyopathy 11 N/A N/A No information
Familial hypertrophic cardiomyopathy 5 N/A N/A No information
Autosomal recessive spastic paraplegia, type 11 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
Primary restless leg syndrome N/A N/A No information
Secondary restless leg syndrome N/A N/A No information
Neurological chronic fatigue syndrome N/A N/A No information
Post-ADD chronic fatigue syndrome N/A N/A No information
Post-viral CFS N/A N/A No information
Infectious CFS N/A N/A No information
Musculoskeletal chronic fatigue syndrome N/A N/A No information
CFS subtype 7 (pain, infectious, musculoskeletal, sleep, neurological, gastrointestinal, neurocognitive, anxiety/depression) N/A N/A No information
CFS subtype 6 (postexertional) N/A N/A No information
CFS subtype 5 (musculoskeletal, gastrointestinal) N/A N/A No information
CFS subtype 4 (cognitive, musculoskeletal, sleep, anxiety/depression) N/A N/A No information
CFS subtype 3 (mild) N/A N/A No information
CFS subtype 2 ( musculoskeletal, pain, anxiety/depression) N/A N/A No information
CFS subtype 1 (cognitive, musculoskeletal, sleep, anxiety/depression) 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
General somatic pain N/A N/A No information
Muscle spasm N/A N/A No information
Distal muscle weakness N/A N/A No information
Contralateral athetosis N/A N/A No information
Mental retardation -- short stature -- hand contractures -- genital anomalies N/A N/A No information
Amyotrophic lateral sclerosis approx 1 in 54,400 or 0.00% or 5,000 people in USA 5,000 estimated 5,000 people are diagnosed with amyotrophic lateral sclerosis in the US, Genetics Home Reference website
Neonatal myasthenia N/A N/A No information
Fibromyalgia 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
Hip muscle strain N/A N/A No information
Lower back muscle strain N/A N/A No information
Thigh muscle strain N/A N/A No information
Eye muscle strain N/A N/A No information
Upper back muscle strain N/A N/A No information
Forearm muscle strain N/A N/A No information
Gluteal muscle strain N/A N/A No information
Hip Flexor strain N/A N/A No information
Groin muscle strain N/A N/A No information
Strain 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
Chronic Fatigue Syndrome N/A N/A No information
Post-polio syndrome N/A N/A No information
Spastic paraparesis N/A N/A No information
Multiple Sclerosis N/A N/A No information
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 No information
Progressive Supranuclear Palsy 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
Achalasia N/A N/A No information
Repetitive Motion Disorders N/A N/A No information
Multifocal motor neuropathy N/A N/A No information
Myopathy N/A N/A No information
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
Type V Glycogen Storage Disease N/A N/A No information
McArdle disease N/A N/A No information
Forbes disease N/A N/A No information
Type IV Glycogen Storage Disease N/A N/A No information
Type VII Glycogen Storage Disease N/A N/A No information
Type III Glycogen Storage Disease N/A N/A No information
Muscular phosphorylase kinase 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
Abdominal muscle strain N/A N/A No information
Bicep muscle strain N/A N/A No information
Leg muscle strain N/A N/A No information
Atonic seizure N/A N/A No information
Focal motor seizure N/A N/A No information
Myoclonic seizures N/A N/A No information
Partial motor seizure N/A N/A No information
Diaphragmatic paralysis N/A N/A No information
Hypnic jerk N/A N/A No information
Calf muscle strain N/A N/A No information
Hand muscle strain N/A N/A No information
Neck muscle strain N/A N/A No information
Muscle strain N/A N/A No information
Clonic seizures N/A N/A No information
Tonic-Clonic seizure N/A N/A No information
Tonic seizure N/A N/A No information
Tricep muscle strain N/A N/A No information
Shoulder muscle strain N/A N/A No information
Respiratory paralysis N/A N/A No information
Upper motor neuron lesions like hyperactive DTRs in the legs N/A N/A No information
Muscle weakness and atrophy as in case of diabetes mellitus N/A N/A No information
Carpal spasm N/A N/A No information
Inability to relax a muscle after its contraction N/A N/A No information
Chronic fatigue syndrome- like myalgia N/A N/A No information
Extraocular muscle palsies N/A N/A No information
Medication induced muscle weakness N/A N/A No information
Choreoathetosis 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
Rheumatic fever-like chorea N/A N/A No information
Cogwheel rigidity 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
Absence of gluteal muscle N/A N/A No information
Osteogenesis imperfecta, type 1A N/A N/A No information
Ehlers-Danlos syndrome type VI N/A N/A No information
Osteogenesis imperfecta Type I 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 No information
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
Complex 5 mitochondrial respiratory chain deficiency 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
Complex 4 mitochondrial respiratory chain deficiency, benign infantile myopathy N/A N/A No information
Complex 4 mitochondrial respiratory chain deficiency, fatal infant myopathy type N/A N/A No information
Complex 4 mitochondrial respiratory chain deficiency N/A N/A No information
Complex 1 mitochondrial respiratory chain deficiency N/A N/A No information
Complex 2 mitochondrial respiratory chain deficiency N/A N/A No information
Parkinsonism, early onset with mental retardation N/A N/A No information
Berardinelli-Seip congenital lipodystrophy N/A N/A No information
Berardinelli-Seip congenital lipodystrophy, type 1 N/A N/A No information
Berardinelli-Seip congenital lipodystrophy, type 2 N/A N/A No information
Mental retardation progressive spasticity, X-linked N/A N/A No information
Spastic disorders N/A N/A No information
Spasticity N/A N/A No information
Cerebral Palsy approx 1 in 34,000 or 0.00% or 8,000 people in USA 8,000 2 to 2.5 per 1,000 births (FMC)
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 No information
Amyotrophic lateral sclerosis, familial type 3 N/A N/A No information
Amyotrophic lateral sclerosis, familial type 4 N/A N/A No information
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 No information
Amyotrophic lateral sclerosis, familial N/A N/A No information
Amyotrophic lateral sclerosis type 1 N/A N/A No information
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
Osteogenesis imperfecta -- congenital joint contractures N/A N/A No information
Osteogenesis imperfecta, type 3 N/A N/A No information
Osteogenesis imperfecta type IIII N/A N/A No information
Tick paralysis N/A N/A No information
Catalepsy N/A N/A No information
Heat cramps N/A N/A No information
Mild cramps N/A N/A No information
Severe muscle pain N/A N/A No information
Temporary paralysis N/A N/A No information
Occasional tremors N/A N/A No information
Glycogen storage disease type 2B -- formerly N/A N/A No information
Pseudoglycogenosis II N/A N/A No information
Glycogen Storage Disease IIb -- formerly N/A N/A No information
GSD2B -- formerly N/A N/A No information
GSD IIB -- formerly N/A N/A No information
Glycogen Storage Disease IXb N/A N/A No information
Glycogen Storage Disease IXa1 N/A N/A No information
Glycogen Storage Disease IXc N/A N/A No information
Type II Glycogen Storage Disease N/A N/A No information
Glycogen storage diseases N/A N/A No information
Glycogen storage disease type 2 N/A N/A No information
Glycogen storage disease type 7 N/A N/A No information
Glycogen storage disease type 2B 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
Congenital Muscular Dystrophy N/A N/A No information
Parkinson disease, juvenile, autosomal recessive N/A N/A No information
Torticollis, familial 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 -- choreoathesis -- abnormal behavior N/A N/A No information
Mental retardation, X-linked -- corpus callosum agenesis -- spastic quadriparesis N/A N/A No information
Mental retardation, X-linked -- epilepsy -- progressive joint contractures -- typical face N/A N/A No information
Mental retardation, X-linked -- craniofacial dysmorphology -- epilepsy -- ophthalmoplegia -- cerebellar atrophy N/A N/A No information
Proximal spinal muscular atrophy, type 3 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
Pyruvate kinase deficiency, muscle type N/A N/A No information
Parkinson disease 10 N/A N/A No information
Parkinson disease 11 N/A N/A No information
Myopathy, Distal 3 N/A N/A No information
Myopathy, Distal 2 N/A N/A No information
Distal Myopathy 1 N/A N/A No information
Muscle cramps N/A N/A No information
Paralytic ileus N/A N/A No information
Torticollis N/A N/A No information
Spasmodic Torticollis N/A N/A No information
Cramp N/A N/A No information
Myopathy -- growth and mental retardation -- hypospadias 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
Myopathy -- growth delay -- mental retardation -- hypospadias N/A N/A No information
Alopecia-contractures-dwarfism-mental retardation N/A N/A No information
Poikilodermatomyositis -- mental retardation 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 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 spastic congenital miosis N/A N/A No information
Athetosis N/A N/A No information
Aural atresia -- multiple congenital anomalies -- mental retardation N/A N/A No information
Macrostomia -- preauricular tags -- external ophthalmoplegia N/A N/A No information
Hypodontia and Dupuytren contracture 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
Lethal arthrogryposis with anterior horn cell disease 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
Cardiomyopathy dilated 1Y N/A N/A No information
Cardiomyopathy dilated 1Z N/A N/A No information
Cardiomyopathy dilated with conduction defect type 1 N/A N/A No information
Cardiomyopathy dilated with conduction defect type 2 N/A N/A No information
Cardiomyopathy, familial dilated N/A N/A No information
Familial dilated cardiomyopathy 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
Progressive external ophthalmoplegia N/A N/A No information
Myoclonus epilepsy N/A N/A No information
Alternating Hemiplegia N/A N/A No information
Motor neuron diseases approx 1 in 49,566 or 0.00% or 5,487 people in USA 5,487 92 annual cases in Victoria 1996 (DHS-VIC)
Dystonias N/A N/A No information
Hemifacial Spasm N/A N/A No information
Hereditary Spastic Paraplegia N/A N/A No information
Progressive muscular atrophy N/A N/A No information
Opsoclonus Myoclonus N/A N/A No information
Quadriplegia N/A N/A No information
Torsion dystonia, X-linked N/A N/A No information
Neurosyphilis -- general paresis N/A N/A No information
Hereditary spastic paralysis, infantile onset ascending N/A N/A No information
Friedreich ataxia N/A N/A No information
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
Neurological causes of muscle weakness N/A N/A No information
Epilepsy-like myoclonic jerks N/A N/A No information
Infectious causes of muscle weakness 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
Sprains and strains N/A N/A No information
Achilles tendon contracture N/A N/A No information
Chvostek's sign N/A N/A No information
Opisthotonos N/A N/A No information
Accessory muscle use N/A N/A No information
Carpopedal spasm N/A N/A No information
Psoas sign N/A N/A No information
Footdrop N/A N/A No information
Orofaciodigital syndrome, type 3 N/A N/A No information
Sugarman syndrome N/A N/A No information
Infantile onset spinocerebellar ataxia N/A N/A No information
Doxorubicin-induced cardiomyopathy N/A N/A No information
Cardiomyopathy due to anthracyclines N/A N/A No information
Juvenile-onset dystonia N/A N/A No information
Chorea familial benign 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
Poland 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
Congenital contractures 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
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
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 No information
Myotonic dystrophy, type 2 N/A N/A No information
Proximal myotonic dystrophy N/A N/A No information
Rhabdomyosarcoma, embryonal 1 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
Idiopathic myopathy N/A N/A No information
Motor neuropathy, peripheral with dysautonomia N/A N/A No information
Multifocal motor neuropathy with conduction block N/A N/A No information
Polymyocytis N/A N/A No information
Myositis N/A N/A No information
Opthalmoplegia -- mental retardation -- lingua scrotalis N/A N/A No information
Tolosa-Hunt Syndrome 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
Myopathy and diabetes mellitus N/A N/A No information
Benign paroxysmal torticollis of infancy 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
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
Ichthyosis mental retardation asymptomatic spasticity 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
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 -- 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
Distal myopathy, Welander type N/A N/A No information
Ossified Ear cartilages with Mental deficiency, Muscle Wasting and Bony Changes N/A N/A No information
Intellectual deficit -- cataracts -- calcified pinnae -- myopathy N/A N/A No information
Aconitase deficiency N/A N/A No information
Myopathy with Exercise Intolerance, Swedish type N/A N/A No information
Myopathy with Deficiency of Succinate Dehydrogenase and Aconitase N/A N/A No information
Myopathy with Lactic Acidosis, Hereditary N/A N/A No information
Cardiomyopathy with myopathy due to COX deficiency N/A N/A No information
Camptodactyly -- joint contractures and facial skeletal dysplasia N/A N/A No information
Lipid storage myopathy N/A N/A No information
Cardiomyopathy -- hypogonadism -- metabolic anomalies N/A N/A No information
Sarcosporidiosis N/A N/A No information
Hypotonia, Seizures and Precocious Puberty N/A N/A No information
Sjogren-Larsson syndrome N/A N/A No information
Tetanus approx 1 in 6,800,000 or 0.00% or 40 people in USA 40 40 annual cases notified in USA 1999 (MMWR 1999); rare due to vaccination.
Congenital SMA with arthrogryposis N/A N/A No information
Oculopharyngeal Muscular Dystrophy N/A N/A No information
Emery-Dreifuss Muscular Dystrophy N/A N/A No information
Distal myopathy with vocal cord weakness N/A N/A No information
Spasmodic dysphonia N/A N/A No information
Spastic dysphonia N/A N/A No information
Woolly hair -- palmoplantar keratoderma -- dilated cardiomyopathy N/A N/A No information
Friedreich ataxia -- congenital glaucoma N/A N/A No information
Ophthalmoplegia N/A N/A No information
Anal sphincter myopathy, internal N/A N/A No information
Ataxia with fasciculations N/A N/A No information
Cardiomyopathy with myopathy due to COX deficency N/A N/A No information
Cardiomyopathy, hypogonadism, collagenoma syndrome N/A N/A No information
Visceral myopathy familial external ophthalmoplegia N/A N/A No information
Myopathy, Mitochonrdrial Progressive, with Congenital Cataract, Hearing Loss and Developmental Delay N/A N/A No information
Myopathy, Myofibrillar, BAG3-Related N/A N/A No information
Myopathy, Congenital, Compton-North N/A N/A No information
Myopathy due to calsequestrin and SERCA1 protein overload N/A N/A No information
Vacuolar Cardiomyopathy and Myopathy, X-linked N/A N/A No information
Myopathy, Distal, with Early Respiratory Failure, Autosomal Dominant N/A N/A No information
Myopathy, Myosin storage N/A N/A No information
Myopathy, hyaline body, autosomal dominant N/A N/A No information
Severe dilated cardiomyopathy with or without myopathy N/A N/A No information
Cardiomyopathy -- hearing loss, type tRNA-LYS gene mutation N/A N/A No information
Cirrhotic cardiomyopathy N/A N/A No information
Hereditary myopathy with intranuclear filamentous N/A N/A No information
Vacuolar myopathy N/A N/A No information
Peripartum cardiomyopathy N/A N/A No information
Distal myopathy with posterior leg and anterior upper limb involvement N/A N/A No information
Hereditary inclusion body myopathy -- joint contractures -- ophthalmoplegia N/A N/A No information
Inclusion body myopathy, type 3 N/A N/A No information
Inclusion body myopathy, type 3, autosomal dominant N/A N/A No information
Inclusion body myopathy, type 3 (IBM3) N/A N/A No information
Myopathy, Congenital, Batten Turner Type N/A N/A No information
Scapuloperoneal amyotrophy N/A N/A No information
Inclusion body myopathy, autosomal dominant N/A N/A No information
Scapuloperoneal myopathy, X-linked dominant 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
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia N/A N/A No information
Cardiomyopathy dilated 3B N/A N/A No information
Cardiomyopathy dilated 2A N/A N/A No information
Atrial cardiomyopathy with heart block N/A N/A No information
Myopathy, early-onset with fatal cardiomyopathy N/A N/A No information
Chagas Cardiomyopathy N/A N/A No information
Myopathy, X-linked with postural muscle atrophy N/A N/A No information
Laing distal myopathy N/A N/A No information
Desmin-related myopathy with Mallory body-like inclusions N/A N/A No information
Cardioencephalomyopathy fatal infantile due to cytochrome c oxidase deficiency N/A N/A No information
Cardiomyopathy, dilated, with Woolly hair and keratoderma N/A N/A No information
Cytoplasmic body myopathy N/A N/A No information
Cardiomyopathy, infantile histiocytoid N/A N/A No information
Amyopathic dermatomyositis N/A N/A No information
Hypertrophic branchial myopathy N/A N/A No information
Brody myopathy N/A N/A No information
Cardiomyopathy, X-linked, fatal infantile N/A N/A No information
Cataract and cardiomyopathy N/A N/A No information
Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation N/A N/A No information
Idiopathic dilation cardiomyopathy N/A N/A No information
Cardiomyopathy, fatal fetal, due to myocardial calcification N/A N/A No information
Cardiomyopathy -- spherocytosis N/A N/A No information
Myopathy -- ophthalmoplegia -- hypoacousia -- areflexia N/A N/A No information
Minicore myopathy, antenatal onset, with arthrogryposis N/A N/A No information
Myopathy, congenital nonprogressive with Moebius and Robin sequences N/A N/A No information
Myopathy mitochondrial -- cataract N/A N/A No information
Myopathy congenital multicore with external ophthalmoplegia N/A N/A No information
Myopathy with lactic acidosis and sideroblastic anemia N/A N/A No information
Native American myopathy N/A N/A No information
Minicore myopathy, moderate, with hand involvement N/A N/A No information
Minicore myopathy with external ophthalmoplegia N/A N/A No information
Inclusion body myopathy 3, autosomal dominant N/A N/A No information
Mitochondrial encephalomyopathy -- aminoacidopathy N/A N/A No information
Mitochondrial myopathy -- lactic acidosis N/A N/A No information
Desmin related myopathy N/A N/A No information
Distal myopathy, Markesbery-Griggs type N/A N/A No information
Hereditary carnitine deficiency syndrome, myopathic N/A N/A No information
Myopathy, X-linked, with excessive autophagy N/A N/A No information
Welander distal myopathy, Swedish type 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
Congenital myopathy N/A N/A No information
Myopathy, myotubular N/A N/A No information
Myopathy, congenital fiber-type disproportion N/A N/A No information
Scapuloperoneal myopathy N/A N/A No information
Centronuclear myopathy, congenital N/A N/A No information
Myopathy with lysis of myofibrils N/A N/A No information
Spheroid body myopathy 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
Bethlem myopathy N/A N/A No information
Myopathy tubular aggregates N/A N/A No information
Miyoshi myopathy N/A N/A No information
Distal myopathy N/A N/A No information
Familial visceral myopathy N/A N/A No information
Genital anomaly -- cardiomyopathy N/A N/A No information
Inclusion body myopathy, 2 autosomal recessive N/A N/A No information
Landouzy-Dejerine muscular dystrophy N/A N/A No information
Batten-Turner 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 No information
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
Scapuloperoneal Syndrome 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
Primary orthostatic tremor N/A N/A No information
Neuroaxonal dystrophy -- renal tubular acidosis N/A N/A No information
Rhabdomyosarcoma, embryonal 2 N/A N/A No information
Ceroid storage disease 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
Smith-Fineman-Myers syndrome 1 N/A N/A No information
Smith-Fineman-Myers syndrome 2 N/A N/A No information
Multicore disease N/A N/A No information
Limb dystonia N/A N/A No information
Franek-Bocker-Kahlen syndrome N/A N/A No information
Microcephaly brain defect spasticity hypernatremia N/A N/A No information
Torsion dystonia with onset in infancy N/A N/A No information
Corpus callosum, agenesis of, blepharophimosis Robin type N/A N/A No information
Spasticity -- multiple exostoses N/A N/A No information
Benign congenital hypotonia N/A N/A No information
Paramyotonia congenita N/A N/A No information
$3-methylglutaconic aciduria, type 1$ N/A N/A No information
$3-methylglutaconic aciduria, type V$ N/A N/A No information
Barth Syndrome N/A N/A No information
Zellweger Syndrome N/A N/A No information
Prader-Willi syndrome N/A N/A No information
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
Craniosynostosis contractures cleft 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
Rippling muscle disease 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
Spasticity -- mental retardation N/A N/A No information
Motor neuropathy N/A N/A No information
Rippling muscle disease, 1 N/A N/A No information
Rippling muscle disease, 2 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
Down Syndrome approx 1 in 800 or 0.12% or 340,000 people in USA 340,000 1-in-800 overall births
Cri-du-chat syndrome N/A N/A No information
Fragile-X Syndrome approx 1 in 3,000 or 0.03% or 90,666 people in USA 90,666 about 1 in 1500 males1.
Huntington's Disease approx 1 in 175,390 or 0.00% or 1,550 people in USA 1,550 26 annual cases in Victoria 1996 (DHS-VIC)
Machado-Joseph Disease N/A N/A No information
Kearns-Sayre Syndrome N/A N/A No information
MELAS 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 1 in 10,000-15,000 live female births
Lafora body disease N/A N/A No information
Benign essential blepharospasm N/A N/A No information
Brachial Plexus Injury N/A N/A No information
Brown-Sequard Syndrome 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
Juvenile dermatomyositis 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
Spasticity -- mental retardation -- epilepsy, X-linked 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
Pompe disease N/A N/A No information
Torsion dystonia N/A N/A No information
Juvenile primary lateral sclerosis N/A N/A No information
Muxcle Phosphoglycerate mutase deficiency N/A N/A No information
Aldolase A 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 No information
Hereditary carnitine deficiency syndrome, systemic N/A N/A No information
Carnitine palmitoyl transferase II deficiency, lethal neonatal form N/A N/A No information
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 No information
Carnitine transporter deficiency N/A N/A No information
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
Respiratory muscle paralysis N/A N/A No information
Chikungunya fever-like intense Muscle aches N/A N/A No information
Rat-bite fever N/A N/A No information
Spirochetes disease N/A N/A No information
Infective myositis N/A N/A No information
Sarcoglycanopathy N/A N/A No information
Bicipital tendinosis N/A N/A No information
Bicipital tendonitis N/A N/A No information
Bicipital syndrome N/A N/A No information
Alpha-sarcoglycanopathy N/A N/A No information
FG syndrome 1 N/A N/A No information
FG syndrome 2 N/A N/A No information
FG syndrome 3 N/A N/A No information
FG syndrome 4 N/A N/A No information
FG syndrome 5 N/A N/A No information
Leiomyoma N/A N/A No information
Leimyoma N/A N/A No information
Sixth nerve palsy, benign N/A N/A No information
Fibrosis of extraocular muscles, congenital, 2 N/A N/A No information
Fibrosis of extraocular muscles, congenital, 3 N/A N/A No information
Fibrosis of extraocular muscles, congenital with synergistic divergence N/A N/A No information
Fibrosis of extraocular muscles, congenital (FEOM) N/A N/A No information
Fibrosis of extraocular muscles, congenital, 1 N/A N/A No information
Benign essential tremor syndrome N/A N/A No information
Delta-sarcoglycanopathy N/A N/A No information
Odontoma -- dysphagia syndrome 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
Narcolepsy with cataplexy N/A N/A No information
Angiopathy, hereditary, with nephropathy, aneurysms and muscle cramps 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
Hypertrophic subaortic stenosis N/A N/A No information
Myodysplasia 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
Hypertrophy and Asymmetry of the Facial Muscles N/A N/A No information
Minicore disease N/A N/A No information
Motor and cognitive disorder due to sepiapterin reductase deficiency N/A N/A No information
Primrose Syndrome N/A N/A No information
Brachydactyly, absent pectoral muscles and agenesis/hypoplasia of kidneys 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
Anterior horn disease N/A N/A No information
Corpus callosum dysgenesis cleft spasm N/A N/A No information
Congenital myasthenic syndromes N/A N/A No information
Multiminicore disease (MmD) N/A N/A No information
Ataxia, episodic -- vertigo -- tinnitus -- myokymia N/A N/A No information
Ossification anomalies -- psychomotor development delay N/A N/A No information
Scapuloperoneal syndrome, neurogenic type N/A N/A No information
Torticollis, keloids, cryptorchidism, renal dysplasia N/A N/A No information
Paraplegia -- brachydactyly -- cone-shaped epiphysis N/A N/A No information
Wolfram's disease N/A N/A No information
Dystrophia myotonica 1 N/A N/A No information
Robinow-Unger syndrome N/A N/A No information
Alport Syndrome N/A N/A No information
Achalasia microcephaly N/A N/A No information
Achalasia, familial esophageal N/A N/A No information
Achalasia -- Addisonianism -- Alacrimia syndrome N/A N/A No information
Achalasia -- alacrimia syndrome N/A N/A No information
Phocomelia -- contractures -- absent thumb N/A N/A No information
Acro-pectoro-renal field defect N/A N/A No information
Spastic paraplegia with precocious puberty N/A N/A No information
Congenital absence of the sternocleidomastoid muscle N/A N/A No information
Contractures -- ectodermal dysplasia -- cleft lip palate N/A N/A No information
Spastic paraparesis deafness N/A N/A No information
Distal hereditary motor neuropathy, type V 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
Severe infantile axonal neuropathy N/A N/A No information
Adrenomyeloneuropathy 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
Idiopathic double athetosis N/A N/A No information
Palmoplantar keratoderma -- amyotrophy N/A N/A No information
Contractures hyperkeratosis lethal N/A N/A No information
Nevo syndrome N/A N/A No information
Ectomorphic Habitus -- Severe Mental Retardation -- Characteristic Face N/A N/A No information
Congenital fiber type disproportion N/A N/A No information
Achalasia -- addisonianism -- alacrima syndrome N/A N/A No information
Achalasia, primary N/A N/A No information
Torsion dystonia, autosomal dominant N/A N/A No information
Hereditary peripheral nervous disorder N/A N/A No information
Ataxia -- oculomotor apraxia, type 1 N/A N/A No information
Tel-Hashomer camptodactyly syndrome N/A N/A No information
Contractures, congenital, torticollis and malignant hyperthermia N/A N/A No information
Muscle phosphoglycerate mutase deficiency N/A N/A No information
Coffin-Lowry syndrome N/A N/A No information
Fahr's Syndrome N/A N/A No information
Inclusion Body Myositis N/A N/A No information
Infantile Spasms N/A N/A No information
Melkersson-Rosenthal Syndrome N/A N/A No information
Hypokalemic periodic paralysis N/A N/A No information
Hyperkalemic periodic paralysis N/A N/A No information
Periodic Paralyses N/A N/A No information
Subacute Sclerosing Panencephalitis N/A N/A No information
Stiff-Person Syndrome N/A N/A No information
Cerebelloparenchymal autosomal recessive disorder 3 N/A N/A No information
Cerebelloparenchymal disorder 3 N/A N/A No information
Cerebelloparenchymal disorder V N/A N/A No information
L1 Syndrome N/A N/A No information
FG Syndrome N/A N/A No information
Cat's cry N/A N/A No information
Congenital torticollis 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
Isaacs syndrome N/A N/A No information
Muscle-eye-brain syndrome N/A N/A No information
Deafness, vitiligo, achalasia 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
Short stature -- contractures -- hypotonia 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
Polyneuropathy -- mental retardation -- acromicria -- premature menopause N/A N/A No information
Myoclonus-ataxia 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
Primerose syndrome 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
Kousseff-Nichols syndrome N/A N/A No information
Pyomyositis N/A N/A No information
Macrogyria, pseudobulbar palsy and mental retardation N/A N/A No information
Marfanoid -- mental retardation syndrome autosomal N/A N/A No information
Neuritis with brachial predilection N/A N/A No information
Pseudomyotonia N/A N/A No information
Lethal congenital contracture syndrome 1 N/A N/A No information
Lethal congenital contracture syndrome 2 N/A N/A No information
Cerebellum agenesis -- hydrocephaly N/A N/A No information
Disorder of Cornification 12 (Neutral Lipid Storage Type) N/A N/A No information
Familial hematuria, autosomal dominant -- retinal arteriolar tortuosity -- contractures 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
Microcephaly micropenis convulsions N/A N/A No information
Degenerative motor system disease N/A N/A No information
Periodic paralysis, potassium-sensitive, cardiodysrythmic type N/A N/A No information
Shprintzen-Golberg craniosynostosis N/A N/A No information
Shprintzen-Goldberg syndrome 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
Facio-cardio-musculo-skeletal syndrome N/A N/A No information
Hypotonia -- failure to thrive -- microcephaly N/A N/A No information
Loeffler's endocarditis N/A N/A No information
Hyperkinesis N/A N/A No information
Alcoholic, reversible acute muscular 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
Ossification anomalies -- psychomotor development N/A N/A No information
Achondroplasia regional -- dysplasia abdominal muscle N/A N/A No information
Leigh syndrome, Saguenay-Lac-St. Jean type N/A N/A No information
Koussef nichols syndrome N/A N/A No information
Lethal congenital contracture syndrome (LCCS) N/A N/A No information
Unusual facies, hypotonia, mental retardation and radioulnar synostosis N/A N/A No information
Limbic encephalitis -- neuromyotonia -- hyperhidrosis -- polyneuropathy N/A N/A No information
Monomelic Amyotrophy N/A N/A No information
Soto's Syndrome approx 1 in 5,000 or 0.02% or 54,400 people in USA 54,399 estimated 1 per 5,000 newborns have Sotos syndrome which includes reported cases and undiagnosed cases, Genetics Home Reference website
Todd's Paralysis N/A N/A No information
Wallenberg's Syndrome N/A N/A No information
Neuromyotonia N/A N/A No information
Cataplexy N/A N/A No information
Intermittent Claudication N/A N/A No information
Tetany N/A N/A No information
Vaginismus N/A N/A No information
Brachial Neuritis N/A N/A No information
Benign Fasciculation Syndrome N/A N/A No information
Rhabdomyolysis N/A N/A No information
Myokymia N/A N/A No information
Walker-Warburg Syndrome N/A N/A No information
Locked-in Syndrome N/A N/A No information
Hyperekplexia N/A N/A No information
Sensorineural hearing loss, early greying, and essential tremor 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
Fibrodysplasia Ossificans Progressiva N/A N/A No information
Lambert-Eaton Myasthenic Syndrome N/A N/A No information
XLMR-Hypotonic Facies Syndrome N/A N/A No information
Wolf-Hirschhorn Syndrome N/A N/A No information
Mulibrey Nanism syndrome N/A N/A No information
Central Core Disease N/A N/A No information
Cohen Syndrome N/A N/A No information
MULIBREY Nanism N/A N/A No information
Schwartz-Jampel Syndrome N/A N/A No information
Neuronal intranuclear hyaline inclusion disease N/A N/A No information
Ophtalmoplegia -- ataxia -- hypoacusis N/A N/A No information
Cutler Syndrome N/A N/A No information
Slavotinek hurst syndrome N/A N/A No information
Saguenay-Lac Saint Jean -- COX deficiency N/A N/A No information
Claudication pain N/A N/A No information
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
Cruse Syndrome N/A N/A No information
Dyck 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
FOSMN syndrome N/A N/A No information
Levy-Yeboa Syndrome N/A N/A No information
MADSAM N/A N/A No information
Mazabraud syndrome N/A N/A No information
Segawa Syndrome N/A N/A No information
Satoyoshi syndrome 2 N/A N/A No information
Spastic pelvic floor syndrome N/A N/A No information
Todd paralysis N/A N/A No information
Zellweger-like syndrome, without peroxisomal anomalies N/A N/A No information
Stiff baby syndrome N/A N/A No information
Verloes-Deprez syndrome N/A N/A No information
Urban rogers meyer syndrome N/A N/A No information
Hedblom syndrome N/A N/A No information
Heerfordt syndrome N/A N/A No information
Keutel syndrome 2 N/A N/A No information
Latham-Munro syndrome N/A N/A No information
Leschke syndrome N/A N/A No information
Lissauer paralysis N/A N/A No information
Lubarsch-Pick syndrome N/A N/A No information
May-White syndrome N/A N/A No information
McLetchie-Aikens syndrome N/A N/A No information
Hemifacial atrophy agenesis of the caudate nucleus N/A N/A No information
Jankovic-Rivera syndrome N/A N/A No information
Filaminopathy, autosomal dominant N/A N/A No information
Coffin syndrome 1 N/A N/A No information
Bruyn-Scheltens syndrome N/A N/A No information
Camera-Marugo-Cohen syndrome N/A N/A No information
Acanthosis nigricans muscle cramps acral enlargement N/A N/A No information
Cramp-fasciculations syndrome N/A N/A No information
Levator syndrome N/A N/A No information
Choreoacanthocytosis amyotrophic N/A N/A No information
Koone-Rizzo-Elias syndrome N/A N/A No information
Dentatorubral pallidoluysian disorder N/A N/A No information
Brushfield-Wyatt syndrome N/A N/A No information
Allen-Masters syndrome N/A N/A No information
Satchmo syndrome N/A N/A No information
Berger paresthesia N/A N/A No information
Bruns-Garland syndrome N/A N/A No information
FACWA syndrome N/A N/A No information
Floppy infant syndrome N/A N/A No information
Foix-Alajouanine syndrome N/A N/A No information
Gamstorp-Wohlfart syndrome N/A N/A No information
Gerlier disease N/A N/A No information
Golden-Lakin syndrome N/A N/A No information
Nguyen syndrome N/A N/A No information
Myoglobinuria recurrent 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
Nakajo-Nishimura syndrome N/A N/A No information
Myoglobinuria, dominant form N/A N/A No information
Supranuclear ocular palsy N/A N/A No information
Passos-Bueno syndrome N/A N/A No information
Myasthenic syndrome, congenital, slow-channel N/A N/A No information
Nondystrophic myotonia N/A N/A No information
Perimyositis N/A N/A No information
Muscular fibrosis, multifocal -- obstructed vessels N/A N/A No information
Nathalie syndrome N/A N/A No information
Fitzsimmons-Walson-Mellor syndrome N/A N/A No information
Emerinopathy N/A N/A No information
Froster-Iskenius-Waterson syndrome N/A N/A No information
Davis-Lafer syndrome N/A N/A No information
Richieri-Costa Da Silva syndrome N/A N/A No information
Dysharmonic skeletal maturation -- muscular fiber disproportion N/A N/A No information
Jung-Wolff-Back-Stahl syndrome N/A N/A No information
Mousa-Al Din-Al Nassar syndrome N/A N/A No information
Developmental delay -- hypotonia extremities hypertrophy 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
Arnold Stickler Bourne syndrome N/A N/A No information
Fanconi-ichthyosis-dysmorphism N/A N/A No information
Snyder-Robinson syndrome N/A N/A No information
TRAPS (TNF-receptor-associated periodic syndrome) N/A N/A No information
Guam disease N/A N/A No information
Lactate dehydrogenase deficiency type B N/A N/A No information
Macrophagic myofasciitis N/A N/A No information
Trigonocephaly -- bifid nose -- acral anomalies N/A N/A No information
Cyprus facial neuromusculoskeletal syndrome N/A N/A No information
Arima syndrome N/A N/A No information
Peptidic growth factors deficiency N/A N/A No information
Medrano-Roldan syndrome N/A N/A No information
Bahemuka Brown syndrome N/A N/A No information
Stoll-Alembik-Finck syndrome N/A N/A No information
Furukawa-Takagi-Nakao syndrome N/A N/A No information
Fernhoff-Blackston-Oakley syndrome N/A N/A No information
Colver-Steer-Godman syndrome N/A N/A No information
Treft-Sanborn-Carey syndrome N/A N/A No information
Satoyoshi syndrome N/A N/A No information
Fitzsimmons-McLachlan-Gilbert syndrome N/A N/A No information
Pitt-Hopkins syndrome N/A N/A No information
Okamuto Satomura syndrome N/A N/A No information
Rhizomelic pseudopolyarthritis N/A N/A No information
Myositis ossificans post-traumatic N/A N/A No information
Pallidopyramidal syndrome N/A N/A No information
Renier-Gabreels-Jasper syndrome N/A N/A No information
Dejerine-Klumpke syndrome N/A N/A No information
Berk-Tabatznik syndrome N/A N/A No information
Ziehen-Oppenheim syndrome N/A N/A No information
Perisylvian syndrome N/A N/A No information
Goldberg-Shprintzen megacolon syndrome N/A N/A No information
Brown-Vialetto-Van Laere syndrome N/A N/A No information
Idiopathic intestinal pseudoobstruction N/A N/A No information
Myoglobinuria N/A N/A No information
BOR-Duane hydrocephalus contiguous gene syndrome N/A N/A No information
Bassoe syndrome N/A N/A No information
Boylan-Dew-Greco syndrome N/A N/A No information
Crisponi syndrome N/A N/A No information
De Grouchy Syndrome N/A N/A No information
Lower limb anomaly -- ureteral obstruction 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
Saul-Wilkes-Stevenson syndrome N/A N/A No information
Opitz-Reynolds-Fitzgerald 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
Reese-Ellsworth syndrome N/A N/A No information
Adrenomyodystrophy N/A N/A No information
Marsden syndrome N/A N/A No information
Small syndrome N/A N/A No information
Di Mauro-Hartlage syndrome N/A N/A No information
Fisher (M.) syndrome N/A N/A No information
Myositis ossificans N/A N/A No information
Prune belly syndrome N/A N/A No information
Megacystis microcolon intestinal hypoperistalsis syndrome N/A N/A No information
Becker disease N/A N/A No information
Erb-Goldflam N/A N/A No information
Kocher-Debre-Semelaigne syndrome N/A N/A No information
Leigh syndrome, French Canadian type N/A N/A No information
Meige syndrome N/A N/A No information
Juberg-Marsidi syndrome N/A N/A No information
Eosinophilia-myalgia syndrome N/A N/A No information
Andersen-Tawil syndrome N/A N/A No information
Brown syndrome N/A N/A No information
Levine-Critchley syndrome N/A N/A No information
Potassium aggravated myotonia N/A N/A No information
Congenital myasthenic syndrome with episodic apnea 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
Winter Harding Hyde syndrome N/A N/A No information
Wells Jankovic syndrome N/A N/A No information
Amyoplasia N/A N/A No information
Amyotonia congenita N/A N/A No information
Oculomelic amyoplasia N/A N/A No information
Lundberg II syndrome N/A N/A No information
Kuskokwim disease N/A N/A No information
Fazio-Londe syndrome N/A N/A No information
Herrmann syndrome N/A N/A No information
Leschke-Ullmann syndrome N/A N/A No information
King-Denborough syndrome N/A N/A No information
Foix-Chavany-Marie syndrome N/A N/A No information
Pseudodiastrophic dysplasia N/A N/A No information
Frontometaphyseal dysplasia N/A N/A No information
Distal arthrogryposis syndrome N/A N/A No information
Hecht syndrome N/A N/A No information
Behr syndrome N/A N/A No information
Wieacker syndrome N/A N/A No information

Types of Muscle conditions

For more information about types of Muscle conditions, refer to our section on types of Muscle conditions.

About incidence:

The medical term 'incidence' of Muscle conditions usually refers to the annual diagnosis rate of new cases of Muscle conditions. Prevalence is a different medical disease measure that refers to the estimated population of people who are managing Muscle conditions at any given time (e.g. prevalence includes people who have had a medical condition for a long time). For more information on prevalence and incidence statistics, see about prevalence and incidence statistics.



Footnotes:
1. Pathophysiology of Disease, Stephen J. McPhee, Vishwanash R. Lingappa, Willim F. Ganong, Jack D. Lang, Prentice Hall, 1995
 

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