DISEASES

Disease-gene associations mined from literature

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Human genes for familial hemiplegic migraine 1

Familial hemiplegic migraine 1 [DOID:0111181]

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

Synonyms:  familial hemiplegic migraine 1,  DOID:0111181,  hereditary hemiplegic migraine 1,  familial hemiplegic migraine1 with progressive cerebellar ataxia,  FHM1 ...

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.