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DO Term : episodic ataxia type 8 [DOID:0050996] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An episodic ataxia that is characterized by weakness, dysarthria and myokymia, and has_material_basis_in autosomal dominant inheritance of mutation in the UBR4 gene.

synonyms:
616055,
OMIM:616055

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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