migraine, with or without aura, susceptibility to, 13
Findings
No curated finding names migraine, with or without aura, susceptibility to, 13 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any migraine disorder in which the cause of the disease is a mutation in the KCNK18 gene.
Definition from the Mondo Disease Ontology (MONDO:0013344), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
2 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Migraine with auraHPOHP:0002077
- Migraine without auraHPOHP:0002083
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- KCNK18HGNC:19439
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Limited · Ambry Genetics · Autosomal dominant · 2018
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2017
- Limited · Laboratory for Molecular Medicine · Unknown · 2020
Where it sits
Other names
3 names
Resolves to: migraine, with or without aura, susceptibility to, 13
- Also called
- KCNK18 migraine disordermigraine disorder caused by mutation in KCNK18migraine, with or without aura, susceptibility to, type 13