Neoplasm of aortic body

Summary

Neoplasm of aortic body (MONDO:0021389) is a cancer. A subtype of aortic disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Classification: Cancer

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	neoplasm of aortic body
Mondo ID	MONDO:0021389
NCIT	C4218
SNOMED CT	127029006
UMLS	C0334417
MedGen	87236
GARD	0025316
Anatomy (UBERON)	UBERON:0034971
Is cancer (heuristic)	yes

Also known as: aortic body neoplasm · aortic body neoplasm (disease) · aortic body paraganglioma · aortic body tumor · aortic body tumour · aorticopulmonary paraganglioma · neoplasm of aortic body · neoplasm of the aortic body · paraganglioma of aortic body · paraganglioma of the aortic body · tumor of aortic body · tumor of the aortic body · tumour of aortic body · tumour of the aortic body

Disease family

This is a subtype of aortic disorder. 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 › vascular disorder › arterial disorder › aortic disorder › neoplasm of aortic body

Related subtypes (16): aortic atherosclerosis, aorta atresia, renal artery disease, superior mesenteric artery syndrome, aortic valve disorder, aortic malignant tumor, aortic aneurysm, tricuspid valve stenosis, aortitis, tricuspid valve prolapse, aorta coarctation, subaortic stenosis, membranous, aneurysm of sinus of Valsalva, Leriche syndrome, X-linked severe syndromic thoracic aortic aneurysm and dissection, fibromuscular dysplasia of the renal arteries

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.