ORPHA:183654
Rare genetic coagulation disorder
- 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 coagulation disorder | |
| fr | Coagulopathie génétique rare | |
| de | Blutgerinnungsstörung, genetisch bedingte, seltene | |
| es | Trastorno raro de coagulación de origen genético | |
| it | Difetto genetico raro della coagulazione | |
| nl | Zeldzame genetische coagulatiestoornis | |
| pt | Coagulopatia genética rara | |
| pl | Rzadkie zaburzenia krzepnięcia uwarunkowane genetycznie | |
| cs | Vzácné geneticky podmíněné poruchy koagulace | |
| uk | Рідкісне генетично обумовлене порушення згортання крові | |
| zh | 罕见遗传性凝血障碍 | |
| tr | Nadir genetik pıhtılaşma bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680533 | 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:158300Rare genetic hematologic disease
rare genetic diseases
Children (5):
- ORPHA:93583Congenital thrombotic thrombocytopenic purpura
- ORPHA:68334Rare hemorrhagic disorder due to a constitutional coagulation factors defect
- ORPHA:71202Rare hemorrhagic disorder due to a constitutional platelet anomaly
- ORPHA:248361Rare thrombotic disorder due to a constitutional coagulation factors defect
- ORPHA:248401Rare thrombotic disorder due to a constitutional platelet anomaly
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/183654
- This record as JSON: /data/d/183654.json