Browse By

Rare (Under 1 in 2000)

Facts
Comparison
ICD-10 Chapter Number
VI 1
ICD-10 Code Range
G00-G99 1
Rare (Under 1 in 2000)
Filter Results52 entries

ALS

Rare (Under 1 in 2000)

Alternating hemiplegia of childhood

Rare (Under 1 in 2000)

Amyotrophic Lateral Sclerosis

Rare (Under 1 in 2000)

Biotin-thiamine-responsive basal ganglia disease

Rare (Under 1 in 2000)

Central core disease

Rare (Under 1 in 2000)

Cerebral folate deficiency

Rare (Under 1 in 2000)

Christianson syndrome

Rare (Under 1 in 2000)

Chronic inflammatory demyelinating polyneuropathy

Rare (Under 1 in 2000)

Cobb syndrome

Rare (Under 1 in 2000)

Dentatorubral-pallidoluysian atrophy

Rare (Under 1 in 2000)

Distal myopathy

Rare (Under 1 in 2000)

Duchenne muscular dystrophy

Rare (Under 1 in 2000)

Familial dysautonomia

Rare (Under 1 in 2000)

Febrile infection-related epilepsy syndrome

Rare (Under 1 in 2000)

Foix-Chavany-Marie Syndrome

Rare (Under 1 in 2000)

Hereditary spastic paraplegia

Rare (Under 1 in 2000)

Hyperkalemic periodic paralysis

Rare (Under 1 in 2000)

Hypokalemic periodic paralysis

Rare (Under 1 in 2000)

Infantile Epileptic Spasms Syndrome

Rare (Under 1 in 2000)

Infantile neuroaxonal dystrophy

Rare (Under 1 in 2000)

Kufor-Rakeb syndrome

Rare (Under 1 in 2000)

Lafora disease

Rare (Under 1 in 2000)

Leigh syndrome

Rare (Under 1 in 2000)

Lennox-Gastaut syndrome

Rare (Under 1 in 2000)

Locked-in syndrome

Rare (Under 1 in 2000)

Machado-Joseph disease

Rare (Under 1 in 2000)

Marinesco-Sjögren syndrome

Rare (Under 1 in 2000)

Metachromatic leukodystrophy

Rare (Under 1 in 2000)

Multifocal motor neuropathy

Rare (Under 1 in 2000)

Multiple System Atrophy

Rare (Under 1 in 2000)

Myasthenia Gravis

Rare (Under 1 in 2000)

Myotonia congenita

Rare (Under 1 in 2000)

Myotonic dystrophy

Rare (Under 1 in 2000)

Nemaline myopathy

Rare (Under 1 in 2000)

Neuroacanthocytosis

Rare (Under 1 in 2000)

Neuroferritinopathy

Rare (Under 1 in 2000)

Neuromyelitis optica spectrum disorder

Rare (Under 1 in 2000)

Pantothenate kinase-associated neurodegeneration

Rare (Under 1 in 2000)

Paroxysmal extreme pain disorder

Rare (Under 1 in 2000)

Paroxysmal kinesigenic dyskinesia

Rare (Under 1 in 2000)

Pelizaeus-Merzbacher disease

Rare (Under 1 in 2000)

Porencephaly

Rare (Under 1 in 2000)

Primary familial brain calcification

Rare (Under 1 in 2000)

Progressive multifocal leukoencephalopathy

Rare (Under 1 in 2000)

Progressive Supranuclear Palsy

Rare (Under 1 in 2000)

Spinocerebellar ataxia type 1

Rare (Under 1 in 2000)

Spinocerebellar ataxia type 13

Rare (Under 1 in 2000)

Spinocerebellar ataxia type 2

Rare (Under 1 in 2000)

Spinocerebellar ataxia type 6

Rare (Under 1 in 2000)

Spinocerebellar ataxia type 7

Rare (Under 1 in 2000)

Showing 1 to 50 of 52, page 1 of 2.

Sources
1. ICD-10 (Wikipedia)
  • ICD-10 chapter table, Chapter VI, chapter number
    VI | G00-G99 | "Diseases of the nervous system"
  • ICD-10 chapter table, Chapter VI, code range
    VI | G00-G99 | "Diseases of the nervous system"
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