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DO Term : spinocerebellar ataxia type 23 [DOID:0050973] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal dominnant cerebellar ataxia that is characterized by slowly progressive ataxia, dysarthria, slow saccades and hyperreflexia, has_material_basis_in mutation in the PDYN gene.

synonyms:
610245,
OMIM:610245

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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