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DOID:0111182 - familial hemiplegic migraine 2
Disease Ontology Definition:A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in ATP1A2 on 1q23.2.
Synonyms: FHM2, Familial hemiplegic migraine-2, MHP2,
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
familial hemiplegic migraine (is_a)