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DO Term : episodic ataxia type 9 [DOID:0060965] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An episodic ataxia that is characterized by onset of ataxic episodes in the first years of life that has_material_basis_in heterozygous mutation in the SCN2A gene on chromosome 2q23.

synonyms:
618924,
OMIM:618924

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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