ORPHA:676036
Peritoneal mesothelioma in situ
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Peritoneal mesothelioma in situ | |
| fr | Mésothéliome péritoine, in situ | |
| de | Peritonealmesotheliom in situ | |
| es | Mesotelioma in situ del peritoneo | |
| it | Mesotelioma peritoneale in situ | |
| nl | Mesothelioom van peritoneum in situ | |
| pt | Mesotelioma peritoneal in situ | |
| pl | Międzybłoniak otrzewnej in situ | |
| cs | Peritoneální mezoteliom in situ | |
| uk | Перитонеальна мезотеліома in situ |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 2C51.20 | NTBT | attributed | validated |
| ICD-11 | 2C51.21 | NTBT | attributed | validated |
| ICD-11 | 2C51.2Y | NTBT | attributed | validated |
| MONDO | 0971145 | E | validated | |
| MONDO | 971145 | E | validated | |
| UMLS | C5925102 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:168807Primary malignant peritoneal tumor
rare abdominal surgical diseases; rare neoplastic diseases; rare transplant-related disorders
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/676036
- This record as JSON: /data/d/676036.json