Familial Hemiplegic Migraine-3

Preferred Label : Familial Hemiplegic Migraine-3;

NCIt synonyms : FHM3;

NCIt definition : An autosomal dominant subtype of familial hemiplegic migraine caused by mutation(s) in the SCN1A gene, encoding sodium channel protein type 1 subunit alpha.;

Details

Origin ID

C205634;

Has associated anatomic sites
- Nervous System [NCIt concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_mapped_to_gene
- SCN1A Gene [NCIt concept]

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