Diseases [C] » Nervous System Diseases [C10] » Neurodegenerative Diseases » Heredodegenerative Disorders, Nervous System
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Heredodegenerative Disorders, Nervous System
Description
Inherited disorders characterized by progressive atrophy and dysfunction of anatomically or physiologically related neurologic systems. MeSH
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Subtype Terms (26)
Alexander Disease
1 experimental drug
Amyloid Neuropathies, Familial
6 drugs (4 approved, 2 experimental)
Bulbo-Spinal Atrophy, X-Linked
5 drugs (4 approved, 1 experimental)
Canavan Disease
6 drugs (3 approved, 3 experimental)
Cockayne Syndrome
1 approved drug
Gerstmann-Straussler-Scheinker Disease
Hepatolenticular Degeneration
20 drugs (10 approved, 10 experimental)
Hereditary Sensory and Autonomic Neuropathies
2 drugs (1 approved, 1 experimental)
Hereditary Sensory and Motor Neuropathy
2 drugs (1 approved, 1 experimental)
Huntington Disease
83 drugs (42 approved, 41 experimental)
Mental Retardation, X-Linked
1 approved drug
Myotonia Congenita
4 approved drugs
Myotonic Dystrophy
13 drugs (6 approved, 7 experimental)
Neurofibromatoses
16 drugs (14 approved, 2 experimental)
Neuronal Ceroid-Lipofuscinoses
15 drugs (5 approved, 10 experimental)
Pantothenate Kinase-Associated Neurodegeneration
2 drugs (1 approved, 1 experimental)
Spinal Muscular Atrophies of Childhood
9 drugs (5 approved, 4 experimental)
Spinocerebellar Degenerations
5 drugs (2 approved, 3 experimental)
Tourette Syndrome
44 drugs (29 approved, 15 experimental)
Tuberous Sclerosis
13 drugs (10 approved, 3 experimental)
Unverricht-Lundborg Syndrome
3 approved drugs
Phase 2 Indicated Drugs (1)
Organization Involved with Phase 2 Indications (1)
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UMLS Data
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