raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:599495

Acquired factor VII deficiency

Type
Disease
Group
Disorder
Inheritance
Not applicable
Age of onset
All ages
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

11 of 12 languages
LangNameSynonyms
enAcquired factor VII deficiency
frDéficit acquis en facteur VII
deFaktor VII-Mangel, erworbener
esDeficiencia del factor VII adquirida
itDeficit acquisito del fattore VII
nlVerworven deficiëntie van factor VII
ptDeficiência de factor VII adquirida
plNabyty niedobór czynnika VII
csZískaný deficit faktoru VII
ukНабутий дефіцит фактора VII
trAcquired factor VII deficiency
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10D68.4NTBTattributedvalidated
ICD-113B2YNTBTindexvalidated
MONDO0035738Evalidated
UMLSC4331989Evalidated

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):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

2 records
TypeClassValueAreaQualificationValidationSource
Cases/families83 casesWorldwideCase(s)Validated36546749[PMID]
Point prevalence<1 / 1 000 000—WorldwideClass onlyValidated36546749[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.

6

HPO phenotypes

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

7

Sources for this card