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Summary Literature (0)
DOID:0111181 - familial hemiplegic migraine 1

Disease Ontology Definition:A familial hemiplegic migraine that is commonly associated with cerebellar degeneration and has_material_basis_in heterozygous mutation in CACNA1A on 19p13.

Synonyms: FHM1, MHP1, familial hemiplegic migraine1 with progressive cerebellar ataxia,

Xenbase Genes : cacna1a



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)