familial hemiplegic migraine 3

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Summary

Literature (0)

DOID:0111183 - familial hemiplegic migraine 3

Disease Ontology Definition:A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in SCN1A on 2q24.3.

Synonyms: FHM3, MHP3,

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

: scn1a

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)