Migraine with aura, susceptibility to, 13

Preferred Label : Migraine with aura, susceptibility to, 13;

Symbol : MGR13;

CISMeF acronym : MGR13;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal Dominant;

Molecular basis : Caused by mutation in the potassium channel, subfamily K, member 18 gene (KCNK18, 613655.0001);

Prefixed ID : #613656;

Details

Origin ID

613656;

UMLS CUI

C4225479;

Genes related to phenotype
- Potassium channel, subfamily k, member 18 [OMIM gene]
HPO term(s)
- Migraine with aura [HPO term]
- Migraine without aura [HPO term]
Semantic type(s)
- Finding [UMLS semantic type]

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