raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRare hemorrhagic disorder due to a constitutional coagulation factors defectRare bleeding disorder due to a constitutional coagulation factors defect · Rare coagulopathy due to a constitutional coagulation factors defect
frMaladie hémorragique rare par déficit constitutionnel en facteurs de coagulationCoagulopathie rare par déficit constitutionnel en facteurs de coagulation
deSeltene Blutgerinnungsstörung durch konstitutionellen Gerinnungsfaktoren-Defekt
esTrastorno hemorrágico raro por un defecto constitucional de factores de coagulaciónCoagulopatía rara por un defecto constitucional de factores de coagulación · Trastorno raro de sangrado por un defecto constitucional de los factores de coagulación
itDisturbo emorragico raro da difetto costituzionale dei fattori della coagulazioneCoagulopatia rara da difetto costituzionale dei fattori della coagulazione
nlZeldzame hemorragische stoornis als gevolg van een constitutionele coagulatiefactordefectZeldzame bloedingsstoornis als gevolg van een constitutionele coagulatiefactorendefect · Zeldzame coagulopathie als gevolg van constitutionele coagulatiefactorendefect
ptDoença hemorragica rara devida a defeito constitucional de factores de coagulaçãoCoagulopatia rara devida a defeito constitucional de factores de coagulação
plRzadkie skazy krwotoczne spowodowane defektami czynników krzepnięciaRare bleeding disorder due to a constitutional coagulation factors defect · Rzadkie koagulopatie spowodowane defektami czynników krzepnięcia
csVzácná hemoragická porucha způsobená konstituční poruchou koagulačních faktorůVzácná krvácivá porucha způsobená konstituční poruchou koagulačních faktorů · Vzácná koagulopatie způsobená konstituční poruchou koagulačních faktorů
ukРідкісне геморагічне захворювання, зумовлене конституційним дефектом факторів згортання кровіРідкісне 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
trYapısal pıhtılaşma faktörleri defektine bağlı nadir hemorajik bozuklukYapısal pıhtılaşma faktörleri defektine bağlı nadir kanama bozukluğu · Yapısal pıhtılaşma faktörleri defektine bağlı nadir koagülopati
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO19039Evalidated
UMLSC5680146Evalidated

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):

Children (18):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card