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Spinocerebellar Ataxia Type 4 (MONDO:0010847)

Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterized by ataxia with sensory neuropathy.

Overview

Category

nervous system disorder

Ontology ID

MONDO:0010847

Internal:11982

Synonyms

SCA4

spinocerebellar ataxia 4

spinocerebellar ataxia autosomal dominant with sensory axonal neuropathy

spinocerebellar ataxia, autosomal dominant, with sensory axonal neuropathy

Mapped terms

DOID:0050957

GARD:0009970

MEDGEN:199815

OMIM:600223

Orphanet:98765

SCTID:715755008

UMLS:C0752122

icd11.foundation:1686006145

Child terms

Unknown children.

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