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migraine, familial hemiplegic, 3
Disease Summary
Associated Targets (1)
Tclin
1
Mondo Description Any familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the SCN1A gene.
Uniprot Description A subtype of migraine associated with transient blindness in some families. Migraine is a disabling symptom complex of periodic headaches, usually temporal and unilateral. Headaches are often accompanied by irritability, nausea, vomiting and photophobia, preceded by constriction of the cranial arteries. The two major subtypes are common migraine (migraine without aura) and classic migraine (migraine with aura). Classic migraine is characterized by recurrent attacks of reversible neurological symptoms (aura) that precede or accompany the headache. Aura may include a combination of sensory disturbances, such as blurred vision, hallucinations, vertigo, numbness and difficulty in concentrating and speaking.
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0111183
GARD:0010974
MESH:C566500
OMIM:609634
UMLS:C1864987
MONDO:0012320
High level summary of knowledge for a disease, including descriptions and datasource references.