ORPHA:140162
Inherited 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 cancer-predisposing syndrome | |
| fr | Syndrome familial avec prédisposition aux cancers | |
| de | Krebsprädispositionssyndrom, hereditäres | Genetisches Tumorprädispositionssyndrom · Hereditäres Tumordispositionssyndrom |
| es | Síndromes de predisposición hereditaria al cáncer | |
| it | Sindrome genetica con predisposizione al cancro | |
| nl | Overgeërfd kankerpredispositiesyndroom | |
| pt | Síndrome predisposição hereditária para cancro | |
| pl | Dziedziczny zespół predyspozycji do nowotworów | |
| cs | Hereditární nádorové syndromy | |
| uk | Успадкований синдром схильності до раку | |
| zh | 遗传性癌症易感综合征 | |
| tr | Kalıtsal kansere yatkınlık sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15356 | E | validated | |
| UMLS | C5680672 | E | validated | |
| GARD | 19921 | 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:98053Rare genetic disease
rare genetic diseases - ORPHA:250908Rare neoplastic disease
rare neoplastic diseases
Children (44):
- ORPHA:289539BAP1-related tumor predisposition syndrome
- ORPHA:1059Blue rubber bleb nevus syndrome
- ORPHA:1359Carney complex
- ORPHA:139411Carney triad
- ORPHA:97286Carney-Stratakis syndrome
- ORPHA:431149Combined immunodeficiency due to OX40 deficiency
- ORPHA:252202Constitutional mismatch repair deficiency syndrome
- ORPHA:284343DICER1 tumor-predisposition syndrome
- ORPHA:1775Dyskeratosis congenita
- ORPHA:615Familial atrial myxoma
- ORPHA:404560Familial atypical multiple mole melanoma syndrome
- ORPHA:313846Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome
- ORPHA:618Familial melanoma
- ORPHA:276399Familial multinodular goiter
- ORPHA:319494Familial nonmedullary thyroid carcinoma
- ORPHA:319487Familial papillary or follicular thyroid carcinoma
- ORPHA:314022Gastric adenocarcinoma and proximal polyposis of the stomach
- ORPHA:377Gorlin syndrome
- ORPHA:145Hereditary breast and/or ovarian cancer syndrome
- ORPHA:26106Hereditary diffuse gastric cancer
- ORPHA:29072Hereditary pheochromocytoma-paraganglioma
- ORPHA:357027Hereditary retinoblastoma
- ORPHA:664450Inherited cancer-predisposing lymphoproliferative syndrome
- ORPHA:425003Inherited digestive cancer-predisposing syndrome
- ORPHA:302Inherited epidermodysplasia verruciformis
- ORPHA:589746Inherited gynecological cancer-predisposing syndrome
- ORPHA:619340Inherited hematologic cancer-predisposing syndrome
- ORPHA:319328Inherited renal cancer-predisposing syndrome
- ORPHA:99749Kostmann syndrome
- ORPHA:661526MBD4-related tumor predisposition syndrome
- ORPHA:293822MITF-related melanoma and renal cell carcinoma predisposition syndrome
- ORPHA:163634Maffucci syndrome
- ORPHA:252206Melanoma and neural system tumor syndrome
- ORPHA:638Neurofibromatosis-Noonan syndrome
- ORPHA:634518Neurofibromatosis/schwannomatosis
- ORPHA:296Ollier disease
- ORPHA:2198Palmoplantar keratoderma-esophageal carcinoma syndrome
- ORPHA:447961Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome
- ORPHA:183422Polymalformative genetic syndrome with increased risk of developing cancer
- ORPHA:435953Progeroid features-hepatocellular carcinoma predisposition syndrome
- ORPHA:692812RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome
- ORPHA:231108Rhabdoid tumor predisposition syndrome
- ORPHA:370396Small cell carcinoma of the ovary
- ORPHA:568056Warts-immunodeficiency-lymphedema-anogenital dysplasia 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/140162
- This record as JSON: /data/d/140162.json