ORPHA:600691

Combined deficiency of factor VII and factor X

Orphadata ships no English definition for this code.

Names in Orphadata languages

10 of 12 languages

Lang	Name	Synonyms
en	Combined deficiency of factor VII and factor X
fr	Déficit combiné en facteurs VII et X
de	Faktor VII und Faktor X, kombinierter Mangel
es	Deficiencia combinada de los factores VII y X
it	Deficit combinato del fattore VII e X
nl	Gecombineerde deficiëntie van factor VII en factor X
pt	Deficiência de factor VII e factor X combinada
pl	Złożony niedobór czynnika VII i X
cs	Kombinovaný deficit faktoru VII a faktoru X
uk	Комбінований дефіцит фактора VII та фактора X

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	D68.2	NTBT	attributed	validated
ICD-11	3B14.2	NTBT	attributed	validated
MONDO	0035776	E		validated
UMLS	C5681529	E		validated

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

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

0 direct

Orphanet records no gene directly on this code.

2 records

Type	Class	Value	Area	Qualification	Validation	Source
Cases/families		7 cases	Worldwide	Case(s)	Validated	28164683[PMID]
Point prevalence	<1 / 1 000 000	—	Worldwide	Class only	Validated	28164683[PMID]_ORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

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