Search Ontology:
Human Disease

episodic ataxia type 8

Term ID
DOID:0050996
Synonyms
Definition
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. https://www.omim.org/entry/616055
References
Ontology
Human Disease   ( DOID:0050996 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models