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DO Term : autosomal recessive spinocerebellar ataxia 24 [DOID:0111615] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the UBA5 gene on chromosome 3q22.1.

synonyms:
617133,
SCAR24,
OMIM:617133

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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