About   Help   FAQ
Disease Ontology Browser
familial hemiplegic migraine 3 (DOID:0111183)
Alliance: disease page
Synonyms: FHM3; MHP3
Alt IDs: OMIM:609634
Definition: A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in SCN1A on 2q24.3.

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory