Long QT syndrome type 6

Preferred Label : Long QT syndrome type 6;

ICD-11 definition : This is an autosomal dominant relatively uncommon form of LQTS. It involves mutations in the gene KCNE2, which encodes for the potassium channel beta subunit MiRP1, constituting part of the IKr repolarizing K current.;

Details

Origin ID

1998894476;

Currated CISMeF NLP mapping
- Long QT syndrome type 6 (disorder) [SNOMED CT concept]
- Long qt syndrome 6 [OMIM Phenotype]
- long QT syndrome 6 [DO Concept]
- long qt syndrome 6 [MeSH Supplementary Concept]
- long qt syndrome 6 [MeSH concept]

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