ORPHA:68334
Rare hemorrhagic disorder due to a constitutional coagulation factors defect
Synonyms: Rare bleeding disorder due to a constitutional coagulation factors defect · Rare coagulopathy due to a constitutional coagulation factors defect
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare hemorrhagic disorder due to a constitutional coagulation factors defect | Rare bleeding disorder due to a constitutional coagulation factors defect · Rare coagulopathy due to a constitutional coagulation factors defect |
| fr | Maladie hémorragique rare par déficit constitutionnel en facteurs de coagulation | Coagulopathie rare par déficit constitutionnel en facteurs de coagulation |
| de | Seltene Blutgerinnungsstörung durch konstitutionellen Gerinnungsfaktoren-Defekt | |
| es | Trastorno hemorrágico raro por un defecto constitucional de factores de coagulación | Coagulopatía rara por un defecto constitucional de factores de coagulación · Trastorno raro de sangrado por un defecto constitucional de los factores de coagulación |
| it | Disturbo emorragico raro da difetto costituzionale dei fattori della coagulazione | Coagulopatia rara da difetto costituzionale dei fattori della coagulazione |
| nl | Zeldzame hemorragische stoornis als gevolg van een constitutionele coagulatiefactordefect | Zeldzame bloedingsstoornis als gevolg van een constitutionele coagulatiefactorendefect · Zeldzame coagulopathie als gevolg van constitutionele coagulatiefactorendefect |
| pt | Doença hemorragica rara devida a defeito constitucional de factores de coagulação | Coagulopatia rara devida a defeito constitucional de factores de coagulação |
| pl | Rzadkie skazy krwotoczne spowodowane defektami czynników krzepnięcia | Rare bleeding disorder due to a constitutional coagulation factors defect · Rzadkie koagulopatie spowodowane defektami czynników krzepnięcia |
| cs | Vzácná hemoragická porucha způsobená konstituční poruchou koagulačních faktorů | Vzácná krvácivá porucha způsobená konstituční poruchou koagulačních faktorů · Vzácná koagulopatie způsobená konstituční poruchou koagulačních faktorů |
| uk | Рідкісне геморагічне захворювання, зумовлене конституційним дефектом факторів згортання крові | Рідкісне порушення згортання крові внаслідок конституціонального дефекту факторів згортання · Рідкісна коагулопатія внаслідок конституціонального дефекту факторів згортання крові |
| zh | 凝血因子缺陷所致罕见出血性疾病 | 体质性凝血因子所致所致罕见凝血病 |
| tr | Yapısal pıhtılaşma faktörleri defektine bağlı nadir hemorajik bozukluk | Yapısal pıhtılaşma faktörleri defektine bağlı nadir kanama bozukluğu · Yapısal pıhtılaşma faktörleri defektine bağlı nadir koagülopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19039 | E | validated | |
| UMLS | C5680146 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:183654Rare genetic coagulation disorder
rare genetic diseases - ORPHA:248315Rare hemorrhagic disorder due to a coagulation factors defect
rare hematological diseases
Children (18):
- ORPHA:35909Combined deficiency of factor V and factor VIII
- ORPHA:600691Combined deficiency of factor VII and factor X
- ORPHA:79Congenital alpha2-antiplasmin deficiency
- ORPHA:326Congenital factor V deficiency
- ORPHA:329Congenital factor XI deficiency
- ORPHA:331Congenital factor XIII deficiency
- ORPHA:335Congenital fibrinogen deficiency
- ORPHA:483Congenital high-molecular-weight kininogen deficiency
- ORPHA:465Congenital plasminogen activator inhibitor type 1 deficiency
- ORPHA:749Congenital prekallikrein deficiency
- ORPHA:169826Congenital vitamin K-dependent coagulation factors deficiency
- ORPHA:599519Factor V short isoforms-related bleeding disorder
- ORPHA:448Hemophilia
- ORPHA:178396Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
- ORPHA:722Hypoplasminogenemia
- ORPHA:3151Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
- ORPHA:436169Thrombomodulin-related bleeding disorder
- ORPHA:903Von Willebrand disease
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/68334
- This record as JSON: /data/d/68334.json