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Human Disease

episodic ataxia type 1

Term ID
DOID:0050989
Synonyms
Definition
An episodic ataxia that is characterized by periodic ataxia and frequent myokymic discharges, and has_material_basis_in autosomal dominant inheritance of mutation in the potassium channel gene KCNA1. https://www.omim.org/entry/160120
References
Ontology
Human Disease   ( DOID:0050989 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models