Atrioventricular dissociation

Summary

Atrioventricular dissociation (MONDO:0008848) is a disease. A subtype of cardiac conduction defect — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	atrioventricular dissociation
Mondo ID	MONDO:0008848
MeSH	D006327
OMIM	209600
ICD-11	268503599
SNOMED CT	50799005
UMLS	C0004331
MedGen	2496
Is cancer (heuristic)	no

Also known as: atrioventricular dissociation · atrioventricular dissociation (disease)

Data availability: 1 HPO phenotype.

Disease family

This is a subtype of cardiac conduction defect. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › cardiovascular disorder › heart disorder › cardiac rhythm disease › cardiac conduction defect › atrioventricular dissociation

Subtypes (2): atrioventricular block, Adams-Stokes syndrome

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 0.