Cor triatriatum dexter
disease diseaseOn this page
Also known as cor triatriatum dexter (disease)cor triatriatum dextrumdivided right atrium
Summary
Cor triatriatum dexter (MONDO:0020429) is a disease. A subtype of triatrial heart — 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 | cor triatriatum dexter |
| Mondo ID | MONDO:0020429 |
| Orphanet | 99098 |
| ICD-11 | 294192583 |
| SNOMED CT | 274947007 |
| UMLS | C0344697 |
| MedGen | 488867 |
| GARD | 0012483 |
| Is cancer (heuristic) | no |
Also known as: cor triatriatum dexter · cor triatriatum dexter (disease) · cor triatriatum dextrum · divided right atrium
Data availability: 1 HPO phenotype.
Disease family
Classification path: disease › human disease › disease by body system or component › cardiovascular disorder › congenital anomaly of cardiovascular system › congenital heart malformation › triatrial heart › cor triatriatum dexter
Related subtypes (1): cor triatriatum sinister
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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.