long QT syndrome 16
MONDO:0032915Mondo
Findings
No curated finding names long QT syndrome 16 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
6 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.
- BradycardiaHPOHP:0001662
- 1 of 1 reported patient · Congenital onset
- Patent ductus arteriosus after birth at termHPOHP:0011648
- 1 of 1 reported patient · Congenital onset
- Perimembranous ventricular septal defectHPOHP:0011682
- 1 of 1 reported patient · Congenital onset
- Prolonged QTc intervalHPOHP:0005184
- 1 of 1 reported patient · Congenital onset
- Second degree atrioventricular blockHPOHP:0011706
- 1 of 1 reported patient · Congenital onset
- T-wave alternansHPOHP:0012266
- 1 of 1 reported patient · Congenital onset
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.
- HGNC:1449HGNC:1449
- Strong · Genomics England PanelApp · Autosomal dominant · 2020
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2022