raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:599490

Acquired factor V deficiency

Type
Disease
Group
Disorder
Inheritance
Not applicable
Age of onset
Adult, Elderly
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

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

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10D68.4NTBTattributedvalidated
ICD-113B2YNTBTindexvalidated
MONDO0035737Evalidated
UMLSC4329256Evalidated
MedDRA10086006Evalidated

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

4 records
TypeClassValueAreaQualificationValidationSource
Point prevalence<1 / 1 000 000—WorldwideClass onlyValidatedORPHANET
Cases/families200 casesWorldwideCase(s)Validated27428013[PMID]_36713339[PMID]_ORPHANET
Annual incidence<1 / 1 000 0000.029 / 100 000AustraliaValue and classValidated15613918[PMID]
Annual incidence<1 / 1 000 0000.009 / 100 000SingaporeValue and classValidated19404538[PMID]

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