ORPHA:619340
Inherited hematologic 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
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Inherited hematologic cancer-predisposing syndrome | |
| fr | Syndrome héréditaire de prédisposition aux cancers hématologiques | |
| de | Krebsprädispositionssyndrom, hämatologisches hereditäres | |
| es | Síndrome de predisposición al cáncer hematológico hereditario | |
| it | Sindrome ereditaria da predisposizione ai tumori ematologici | |
| nl | Erfelijke hematologische kanker-predispositiesyndroom | |
| pt | Síndrome de predisposição a cancro hematológico hereditário | |
| pl | Wrodzony zespół predyspozycji do nowotworów układu krwiotwórczego | |
| cs | Dědičný syndromy predisponující k hematologické malignitě | |
| uk | Спадковий синдром схильності до раку крові |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0850064 | E | validated | |
| UMLS | C5681832 | 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:140162Inherited cancer-predisposing syndrome
rare genetic diseases; rare neoplastic diseases
Children (8):
- ORPHA:697385Combined immunodeficiency-cancer predisposing syndrome due to AIOLOS deficiency
- ORPHA:488647DDX41-related hematologic malignancy predisposition syndrome
- ORPHA:697414Early-onset combined immunodeficiency with low Ig due to dominant negative IKAROS mutation
- ORPHA:71290Familial platelet disorder with associated myeloid malignancy
- ORPHA:319465Inherited acute myeloid leukemia
- ORPHA:524Li-Fraumeni syndrome
- ORPHA:648Noonan syndrome
- ORPHA:500Noonan syndrome with multiple lentigines
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/619340
- This record as JSON: /data/d/619340.json