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bn:00908964n
Noun Concept
Categories: Central nervous system disorders, Neurogenetic disorders, Autosomal dominant disorders, Trinucleotide repeat disorders
EN
dentatorubral-pallidoluysian atrophy  dentatorubral–pallidoluysian atrophy  Ataxia, Chorea, Seizures, and Dementia  DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY; DRPLA  Dentatorubral pallidoluysian atrophy
EN
Dentatorubral–pallidoluysian atrophy is an autosomal dominant spinocerebellar degeneration caused by an expansion of a CAG repeat encoding a polyglutamine tract in the atrophin-1 protein. Wikipedia
Definitions
Relations
Sources
EN
Dentatorubral–pallidoluysian atrophy is an autosomal dominant spinocerebellar degeneration caused by an expansion of a CAG repeat encoding a polyglutamine tract in the atrophin-1 protein. Wikipedia
Congenital disorder of nervous system Wikidata
IS A
disease
rare disease
spinocerebellar ataxia
Huntington's disease-like syndrome
GENETIC ASSOCIATION
ATN1
HEALTH SPECIALTY
neurology
Wikipedia
EN
dentatorubral–pallidoluysian atrophy
Wikidata
EN
dentatorubral-pallidoluysian atrophy
Wikipedia Redirections
EN
dentatorubral-pallidoluysian atrophy, dentatorubral pallidoluysian atrophy, dentatorubropallidoluysian atrophy, DRPLA
Wikidata Alias
EN
Ataxia, Chorea, Seizures, and Dementia, DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY, DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY; DRPLA, Dentatorubral pallidoluysian atrophy, Dentatorubropallidoluysian atrophy, DRPLA, Haw River Syndrome, Myoclonic Epilepsy With Choreoathetosis, Naito-Oyanagi disease, Naito Oyanagi disease, NOD

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