ORPHA:248368
Rare thrombotic disorder due to a platelet anomaly
- 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 thrombotic disorder due to a platelet anomaly | |
| fr | Maladie thrombotique rare par anomalie des plaquettes | |
| de | Seltene thrombotische Störung durch Blutplättchenanomalie | |
| es | Enfermedad trombótica rara por anomalía de las plaquetas | |
| it | Disturbo trombotico raro da difetto piastrinico | |
| nl | Zeldzame trombotische stoornis als gevolg van een bloedplaatjesanomalie | |
| pt | Doença trombótica rara por anomalia de plaquetas | |
| pl | Rzadkie zaburzenie krzepnięcia z powodu anomalii płytek krwi | |
| cs | Vzácné poruchy srážlivosti způsobené anomáliemi destiček | |
| uk | Рідкісний тромботичний розлад, зумовлений аномалією тромбоцитів | |
| zh | 血小板异常所致罕见性血栓性疾病 | |
| tr | Trombosit anomalisine bağlı nadir trombotik bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16635 | E | validated | |
| UMLS | C5680687 | 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:182054Rare thrombotic disease of hematologic origin
rare hematological diseases
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/248368
- This record as JSON: /data/d/248368.json