heart conduction disease
MONDO:0000992Mondo
Findings
No curated finding names heart conduction disease yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A disease that has its basis in the disruption of the heart's electrical conduction system.
Definition from the Mondo Disease Ontology (MONDO:0000992), read 2026-09-29. CC BY 4.0.
Genes
10 genes
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.
- EMDHGNC:3331
- Strong · Genomics England PanelApp · X-linked · 2020
- TTRHGNC:12405
- Strong · Genomics England PanelApp · Autosomal dominant · 2020
- CLCA2HGNC:2016
- Moderate · Genomics England PanelApp · Autosomal dominant · 2020
- TBX5HGNC:11604
- Moderate · Genomics England PanelApp · Autosomal dominant · 2020
- ACTN2HGNC:164
- Limited · Genomics England PanelApp · Autosomal dominant · 2020
- ANK2HGNC:493
- Limited · Genomics England PanelApp · Autosomal dominant · 2020
- FLNCHGNC:3756
- Limited · Genomics England PanelApp · Autosomal dominant · 2020
- GJA5HGNC:4279
- Limited · Genomics England PanelApp · Autosomal dominant · 2020
- KCNK17HGNC:14465
- Limited · Genomics England PanelApp · Unknown · 2020
- TBX3HGNC:11602
- Limited · Genomics England PanelApp · Autosomal dominant · 2020
Where it sits
- A kind of
- Narrower terms (10)
- atrioventricular block
- Brugada syndrome
- catecholaminergic polymorphic ventricular tachycardia
- NKX2.5-related congenital, conduction and myopathic heart disease
- postural orthostatic tachycardia syndrome due to NET deficiency
- progressive familial heart block
- short QT syndrome
- sinoatrial block
- sinoatrial node disorder
- Wolff-Parkinson-White syndrome
Other names
5 names
Resolves to: heart conduction disease
- Also called
- cardiac conduction diseasecardiac conduction disorderconduction disease of heartdisease of cardiac conductiondisorder of cardiac conduction