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Echinobase
Summary Literature (0)
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,

Echinobase Genes :


OMIM:
MIM:602481 - migraine, familial hemiplegic, 2; fhm2

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): familial hemiplegic migraine (is_a)