Benign peritoneal mesothelioma

Summary

Benign peritoneal mesothelioma (MONDO:0002112) is a disease. A subtype of peritoneal benign neoplasm — 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 peritoneal mesothelioma
Mondo ID	MONDO:0002112
DOID	DOID:1789
NCIT	C7354
UMLS	C0346113
MedGen	87540
Anatomy (UBERON)	UBERON:0002358
Is cancer (heuristic)	no

Also known as: mesothelioma of peritoneum · peritoneal adenomatoid tumor · peritoneal adenomatoid tumour · peritoneum benign mesothelioma

Disease family

This is a subtype of peritoneal benign neoplasm. 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 › benign neoplasm › peritoneal benign neoplasm › benign peritoneal mesothelioma

Related subtypes (2): disseminated peritoneal leiomyomatosis, benign peritoneal solitary fibrous tumor

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.