benign PEComa

Summary

benign PEComa (MONDO:0020581) is a disease. A subtype of neoplasm with perivascular epithelioid cell differentiation — 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	benign PEComa
Mondo ID	MONDO:0020581
NCIT	C121791
UMLS	C3839685
MedGen	825530
GARD	0025175
Is cancer (heuristic)	no

Also known as: benign neoplasm with perivascular epithelioid cell differentiation · benign PEComa · benign PEComa, nos · benign PEComa, not otherwise specified · neoplasm with perivascular epithelioid cell differentiation, benign · typical PEComa

Disease family

This is a subtype of neoplasm with perivascular epithelioid cell differentiation. 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 › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › connective and soft tissue neoplasm › soft tissue neoplasm › neoplasm with perivascular epithelioid cell differentiation › benign PEComa

Related subtypes (5): angiomyolipoma, uterine corpus perivascular epithelioid cell tumor, lymphangiomyoma, lymphangioleiomyomatosis, lung PEComa

Subtypes (2): clear cell-sugar-tumor of the lung, kidney angiomyolipoma

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.