ORPHA:68336
Rare genetic 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare genetic tumor | |
| fr | Tumeur génétique rare | |
| de | Tumor, seltener, genetisch bedingter | |
| es | Tumor genético raro | |
| it | Tumore genetico | |
| nl | Zeldzame genetische tumor | |
| pt | Tumor genético raro | |
| pl | Rzadkie guzy genetyczne | |
| cs | Vzácné geneticky podmíněné nádory | |
| uk | Рідкісна генетично обумовлена пухлина | |
| zh | 罕见基因型肿瘤 | |
| tr | Nadir genetik tümör |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19041 | E | validated | |
| UMLS | C5681311 | 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:98053Rare genetic disease
rare genetic diseases
Children (11):
- ORPHA:183527Genetic bone tumor
- ORPHA:271841Genetic cardiac tumor
- ORPHA:271835Genetic digestive tract tumor
- ORPHA:183619Genetic eye tumor
- ORPHA:183734Genetic gynecological tumor
- ORPHA:271847Genetic neuroendocrine tumor
- ORPHA:183595Genetic renal tumor
- ORPHA:183487Genetic skin tumor or hamartoma
- ORPHA:271832Genetic soft tissue tumor
- ORPHA:322126Genetic tumor of hematopoietic and lymphoid tissues
- ORPHA:271844Genetic urogenital tumor
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/68336
- This record as JSON: /data/d/68336.json