ORPHA:168807
Primary malignant peritoneal tumor
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Primary malignant peritoneal tumor | |
| fr | Tumeur péritonéale primaire maligne | |
| de | Peritonealtumor, maligner primärer | |
| es | Tumor primario peritoneal maligno | |
| it | Tumore peritoneale maligno primario | |
| nl | Maligne primaire peritoneale tumor | Kwaadaardige primaire peritoneale tumor |
| pt | Tumor peritoneal maligno primário | |
| pl | Pierwotny złośliwy guz otrzewnej | |
| cs | Primární maligní peritoneální nádory | |
| uk | Первинна злоякісна перитоніальна пухлина | |
| zh | 原发性恶性腹膜肿瘤 | |
| tr | Primer habis peritoneal tümör |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15683 | E | validated | |
| UMLS | C5680454 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:168803Primary peritoneal tumor
rare abdominal surgical diseases; rare neoplastic diseases - ORPHA:506216Rare disorder potentially indicated for bowel transplant
rare transplant-related disorders
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/168807
- This record as JSON: /data/d/168807.json