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migraine, with or without aura, susceptibility to, 13
Disease Summary
Associated Targets (1)
Tclin
1
Mondo Description Any migraine disorder in which the cause of the disease is a mutation in the KCNK18 gene.
Uniprot Description A form of migraine transmitted in an autosomal dominant pattern. 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.
Mondo Term and Equivalent IDs
MONDO:0013344: migraine, with or without aura, susceptibility to, 13
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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.
OMIM:613656
MONDO:0013344
High level summary of knowledge for a disease, including descriptions and datasource references.