ORPHA:169826

Congenital vitamin K-dependent coagulation factors deficiency

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.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Congenital vitamin K-dependent coagulation factors deficiency
fr	Déficit congénital en facteurs Vitamino-K dépendants
de	Vitamin K-abhängige Gerinnungsfaktoren, kongenitaler Mangel
es	Factores de coagulación vitamina K-dependientes congénitos
it	Fattori di coagulazione congeniti dipendenti dalla vitamina K
nl	Congenitale deficiëntie van vitamine K-afhankelijke stollingsfactoren
pt	Deficiência congénita de fatores de coagulação dependentes da vitamina K
pl	Wrodzony Niedobór czynników krzepnięcia zależny od witaminy K
cs	Vrozený deficit koagulačních faktorů závislých na vitaminu K
uk	Вроджений дефіцит вітамін К-залежних факторів згортання крові
zh	先天性维生素K依赖凝血因子缺乏症
tr	Doğumsal K vitaminine bağlı pıhtılaşma faktörleri eksikliği

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	15722	E		validated
UMLS	C5680448	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:97992Rare hematologic disease

Parents in the classifications (1):

ORPHA:68334Rare hemorrhagic disorder due to a constitutional coagulation factors defect
rare genetic diseases; rare hematological diseases

Children (4):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

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

Sources for this card

Orphanet page: orpha.net/en/disease/detail/169826
This record as JSON: /data/d/169826.json