familial hemiplegic migraine 1 Disease Ontology Browser

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Disease Ontology Browser

familial hemiplegic migraine 1 (DOID:0111181)
Alliance: disease page
Synonyms: familial hemiplegic migraine1 with progressive cerebellar ataxia; FHM1; MHP1
Alt IDs: OMIM:141500
Definition: A familial hemiplegic migraine that is commonly associated with cerebellar degeneration and has_material_basis_in heterozygous mutation in CACNA1A on 19p13.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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