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familial hemiplegic migraine 2 (DOID:0111182)
Alliance: disease page
Synonyms: Familial hemiplegic migraine-2; FHM2; MHP2
Alt IDs: OMIM:602481
Definition: A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in ATP1A2 on 1q23.2.

Disease References using Mouse Models (4)
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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory