Aortic aneurysm, familial abdominal, 2

Summary

Aortic aneurysm, familial abdominal, 2 (MONDO:0012343) is a disease. A subtype of familial abdominal aortic aneurysm — 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	aortic aneurysm, familial abdominal, 2
Mondo ID	MONDO:0012343
MeSH	C565229
OMIM	609782
UMLS	C1853364
MedGen	339960
GARD	0016492
Is cancer (heuristic)	no

Also known as: AAA2 · aortic aneurysm, familial abdominal 2 · aortic aneurysm, familial abdominal, 2

Disease family

This is a subtype of familial abdominal aortic aneurysm. 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 etiologic mechanism › disease of genetic or genomic mechanism › hereditary disease › familial abdominal aortic aneurysm › aortic aneurysm, familial abdominal, 2

Related subtypes (3): aortic aneurysm, familial abdominal, 3, aortic aneurysm, familial abdominal, 4, aortic aneurysm, familial abdominal, 1

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.