Mesh term Heredodegenerative Disorders, Nervous System
Browse to parent terms:Genetic Diseases, Inborn
Neurodegenerative Diseases
Description
Inherited disorders characterized by progressive atrophy and dysfunction of anatomically or physiologically related neurologic systems.Browse to child terms:
Alexander Disease
Amyloid Neuropathies, Familial
Bulbo-Spinal Atrophy, X-Linked
Canavan Disease
Cockayne Syndrome
Dystonia Musculorum Deformans
Gerstmann-Straussler-Scheinker Disease
Hepatolenticular Degeneration
Hereditary Central Nervous System Demyelinating Diseases
Hereditary Sensory and Autonomic Neuropathies
Hereditary Sensory and Motor Neuropathy
Huntington Disease
Lafora Disease
Mental Retardation, X-Linked
Myotonia Congenita
Myotonic Dystrophy
Neuroacanthocytosis
Neurofibromatoses
Neuronal Ceroid-Lipofuscinoses
Optic Atrophies, Hereditary
Pantothenate Kinase-Associated Neurodegeneration
Spinal Muscular Atrophies of Childhood
Spinocerebellar Degenerations
Tourette Syndrome
Tuberous Sclerosis
Unverricht-Lundborg Syndrome
Search for this term in our Faculty Database
View this term at the NCBI website