ORPHA:180257
Rare malignant breast tumor
Synonyms: Rare breast cancer
- 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 | Rare malignant breast tumor | Rare breast cancer |
| fr | Tumeurs malignes rare du sein | Cancer rare du sein |
| de | Seltener maligner Tumor der Brust | Seltener Brustkrebs |
| es | Tumor maligno raro de mama | Cáncer de mama raro |
| it | Tumore maligno raro della mammella | Cancro raro della mammella |
| nl | Zeldzame maligne borsttumor | Zeldzame borstkanker · Zeldzame kwaadaardige borsttumor |
| pt | Cancro da mama maligno, raro | |
| pl | Rzadki złośliwy guz piersi | Rzadki rak piersi |
| cs | Vzácné zhoubné nádory prsu | = en |
| uk | Рідкісна злоякісна пухлина молочної залози | Рідкісний рак молочної залози |
| zh | 罕见乳房恶性肿瘤 | 罕见乳腺癌 |
| tr | Nadir görülen habis meme tümörü | Nadir meme kanseri |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15870 | E | validated | |
| UMLS | C5679588 | 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 (1):
- ORPHA:180250Rare breast tumor
rare neoplastic diseases; rare gynecological and obstetric diseases
Children (7):
- ORPHA:145Hereditary breast and/or ovarian cancer syndrome
- ORPHA:694963Inflammatory breast cancer
- ORPHA:213531Metaplastic carcinoma of the breast
- ORPHA:180275Paget disease of the nipple
- ORPHA:180261Phyllodes tumor of the breast
- ORPHA:213528Rare adenocarcinoma of the breast
- ORPHA:213557Salivary gland type cancer of the breast
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/180257
- This record as JSON: /data/d/180257.json