Well differentiated papillary mesothelioma
diseaseOn this page
Also known as benign/Intermediate mesotheliomaWDPMwell-differentiated mesothelial papillary neoplasmwell-differentiated mesothelial papillary tumorwell-differentiated mesothelial papillary tumourwell-differentiated papillary neoplasm of mesotheliumwell-differentiated papillary neoplasm of the mesotheliumwell-differentiated papillary tumor of mesotheliumwell-differentiated papillary tumor of the mesotheliumwell-differentiated papillary tumour of mesotheliumwell-differentiated papillary tumour of the mesothelium
Summary
Well differentiated papillary mesothelioma (MONDO:0003688) is a disease. A subtype of mesothelioma — 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 | well differentiated papillary mesothelioma |
| Mondo ID | MONDO:0003688 |
| DOID | DOID:5884 |
| NCIT | C7635 |
| UMLS | C1337012 |
| MedGen | 234487 |
| Is cancer (heuristic) | no |
Also known as: benign/Intermediate mesothelioma · WDPM · well differentiated papillary mesothelioma · well-differentiated mesothelial papillary neoplasm · well-differentiated mesothelial papillary tumor · well-differentiated mesothelial papillary tumour · well-differentiated papillary neoplasm of mesothelium · well-differentiated papillary neoplasm of the mesothelium · well-differentiated papillary tumor of mesothelium · well-differentiated papillary tumor of the mesothelium · well-differentiated papillary tumour of mesothelium · well-differentiated papillary tumour of the mesothelium
Disease family
This is a subtype of 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 › well differentiated papillary mesothelioma
Related subtypes (6): benign mesothelioma, pleural mesothelioma, adenomatoid tumor, malignant mesothelioma, peritoneal mesothelioma, well-differentiated papillary mesothelial tumour of the pleura
Subtypes (1): peritoneal well differentiated papillary mesothelioma
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.