Peritoneal multicystic mesothelioma
diseaseOn this page
Also known as benign cystic peritoneal mesotheliomabenign multicystic peritoneal mesotheliomaBMPMmulticystic mesotheliomamulticystic mesothelioma of peritoneummulticystic mesothelioma of the peritoneummultilocular peritoneal cystsmultilocular peritoneal inclusion cystmultilocular peritoneal inclusion cystsperitoneal cystic mesothelioma
Summary
Peritoneal multicystic mesothelioma (MONDO:0006363) is a disease. A subtype of peritoneal mesothelioma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Prevalence: Unknown (Worldwide) [Orphanet-validated]
- Phenotypes (HPO): 9
Clinical features
Epidemiology
Prevalence records
1 prevalence record(s), Orphanet:
| Type | Class | Value | Geography | Validation |
|---|---|---|---|---|
| Cases/families | 150 | Worldwide | Validated |
Signs & symptoms
Clinical features (HPO)
9 HPO clinical features (Orphanet curated; top 9 by frequency):
| HPO ID | Term | Frequency |
|---|---|---|
| HP:0002019 | Constipation | Very frequent (80-99%) |
| HP:0002027 | Abdominal pain | Very frequent (80-99%) |
| HP:0002586 | Peritonitis | Very frequent (80-99%) |
| HP:0002664 | Neoplasm | Very frequent (80-99%) |
| HP:0003270 | Abdominal distention | Very frequent (80-99%) |
| HP:0000132 | Menorrhagia | Frequent (30-79%) |
| HP:0001824 | Weight loss | Frequent (30-79%) |
| HP:0030016 | Dyspareunia | Frequent (30-79%) |
| HP:0100608 | Metrorrhagia | Frequent (30-79%) |
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | peritoneal multicystic mesothelioma |
| Mondo ID | MONDO:0006363 |
| EFO | EFO:1000468 |
| Orphanet | 168816 |
| NCIT | C6536 |
| SNOMED CT | 716650003 |
| UMLS | C1334818 |
| MedGen | 233198 |
| GARD | 0010777 |
| Is cancer (heuristic) | no |
Also known as: benign cystic peritoneal mesothelioma · benign multicystic peritoneal mesothelioma · BMPM · multicystic mesothelioma · multicystic mesothelioma of peritoneum · multicystic mesothelioma of the peritoneum · multilocular peritoneal cysts · multilocular peritoneal inclusion cyst · multilocular peritoneal inclusion cysts · peritoneal cystic mesothelioma · peritoneal multicystic mesothelioma
Disease family
This is a subtype of peritoneal mesothelioma. 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 › mesothelial neoplasm › mesothelioma › peritoneal mesothelioma › peritoneal multicystic mesothelioma
Related subtypes (4): benign peritoneal mesothelioma, malignant peritoneal mesothelioma, peritoneal well differentiated papillary mesothelioma, peritoneal mesothelioma in situ
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.