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DO Term : spinocerebellar ataxia type 12 [DOID:0050962] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal dominant cerebellar ataxia that is characterized by minor ataxia and intention tremor, has_material_basis_in CAG expansion of the PPP2R2B gene.

synonyms:
604326,
OMIM:604326

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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