ORPHA:319328
Inherited renal cancer-predisposing syndrome
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Inherited renal cancer-predisposing syndrome | |
| fr | Syndrome héréditaire de prédisposition aux cancers rénaux | Syndrome familial avec prédisposition aux cancers du rein |
| de | Vererbtes Nierenzell-Krebsprädispositionssyndrom | |
| es | Síndrome de predisposición hereditaria al cáncer de células renales | |
| it | Sindrome ereditaria da predisposizione al cancro delle cellule renali | |
| nl | Overgeërfde niercelkanker-predispositiesyndroom | |
| pt | Síndrome hereditária de predisposição ao cancro de células renais | |
| pl | Wrodzony zespół predyspozycji do nowotworu nerki | |
| cs | Dědičný syndrom predispozice k rakovině ledvin | |
| uk | Спадковий синдром схильності до раку нирок | |
| zh | 遗传性肾癌易感综合征 | |
| tr | Kalıtsal böbrek kanserine yatkınlık sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17891 | E | validated | |
| UMLS | C5680964 | 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 (2):
- ORPHA:140162Inherited cancer-predisposing syndrome
rare genetic diseases; rare neoplastic diseases - ORPHA:93626Rare renal disease
rare renal diseases
Children (13):
- ORPHA:116Beckwith-Wiedemann syndrome
- ORPHA:122Birt-Hogg-Dubé syndrome
- ORPHA:97290Familial papillary thyroid carcinoma with renal papillary neoplasia
- ORPHA:404476Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome
- ORPHA:422526Hereditary clear cell renal cell carcinoma
- ORPHA:523Hereditary leiomyomatosis and renal cell cancer
- ORPHA:47044Hereditary papillary renal cell carcinoma
- ORPHA:99880Hyperparathyroidism-jaw tumor syndrome
- ORPHA:319462Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
- ORPHA:2849Perlman syndrome
- ORPHA:805Tuberous sclerosis complex
- ORPHA:892Von Hippel-Lindau disease
- ORPHA:893WAGR syndrome
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/319328
- This record as JSON: /data/d/319328.json