ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome
MONDO:0020745Mondo
Findings
No curated finding names ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
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.
- Left ventricular noncompaction cardiomyopathyHPOHP:0011664
- 2 of 46 reported patients
- Torsade de pointesHPOHP:0001664
- 1 of 46 reported patients
- Aborted sudden cardiac deathHPOHP:0031628
- Polymorphic and polytopic ventricular extrasystolesHPOHP:0006696
- Sudden cardiac deathHPOHP:0001645
- Ventricular fibrillationHPOHP:0001663
Where it sits
Other names
2 names
Resolves to: ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome
- Also called
- autosomal dominant cardiac arrhythmia (Kuhn)VACRDS