Long qt syndrome 16

Preferred Label : Long qt syndrome 16;

Symbol : LQT16;

CISMeF acronym : LQT16;

Type : Phenotype, molecular basis known;

Included titles and symbols : Ventricular tachycardia, catecholaminergic polymorphic 6; CPVT6;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the calmodulin-3 gene (CALM3, 114183.0001);

Prefixed ID : #618782;

Details

Origin ID

618782;

UMLS CUI

C5394068;

Genes related to phenotype
- Calmodulin 3 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Bradycardia [HPO term]
- Patent ductus arteriosus after birth at term [HPO term]
- Perimembranous ventricular septal defect [HPO term]
- Prolonged QTc interval [HPO term]
- Second degree atrioventricular block [HPO term]
- T-wave alternans [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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