juvenile myoclonic epilepsy 10

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Summary

Literature (0)

DOID:0111325 - juvenile myoclonic epilepsy 10

Disease Ontology Definition:A juvenile myoclonic epilepsy that has_material_basis_in heterozygous mutation in ICK on chromosome 6p12.1.

Synonyms: EJM10,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): juvenile myoclonic epilepsy (is_a)