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DO Term : episodic ataxia type 5 [DOID:0050993] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  An episodic ataxia that is characterized by dysarthria and vertigo, develops in early childhood, and has_material_basis_in autosomal dominant inheritance of mutation in the CACNB4 gene.
  • synonyms:
  • 613855,
  • OMIM:613855
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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