episodic ataxia type 5 Disease Ontology Browser

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Disease Ontology Browser

episodic ataxia type 5 (DOID:0050993)
Alliance: disease page
Alt IDs: OMIM:613855
Definition: 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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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