raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:599480

Acquired hemophilia A

Synonyms: AHA · Acquired F8 deficiency · Acquired factor VIII deficiency

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

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

10 of 12 languages
LangNameSynonyms
enAcquired hemophilia AAHA · Acquired F8 deficiency · Acquired factor VIII deficiency
frHémophilie acquise ADéficit acquis en F8 · Déficit acquis en facteur VIII
deHämophilie A, erworbeneAHA · F8-Mangel, erworbener · Faktor VIII-Mangel, erworbener
esHemofilia A adquiridaDeficiencia adquirida de F8 · Deficiencia adquirida de factor VIII · HAA
itEmofilia A acquisitaAHA · Deficit acquisito del fattore VIII · Deficit acquisito di F8
nlVerworven hemofilie AAHA · Verworven F8-deficiëntie · Verworven deficiëntie van factor VIII
ptHemofilia A adquiridaDeficiência adquirida de F8 · Deficiência adquirida de factor VIII · HAA
plNabyta hemofilia AAHA
csZískaná hemofilie A= en
ukНабута гемофілія АНабута недостатність F8 · Набутий дефіцит фактора VIII · AHA
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10D68.4NTBTattributedvalidated
ICD-113B22NTBTindexvalidated
MONDO0035735Evalidated
MeSHC536392Evalidated
UMLSC0272325Evalidated
GARD6405Evalidated
MedDRA10082745Evalidated

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

14 records
TypeClassValueAreaQualificationValidationSource
Annual incidence1-9 / 1 000 0000.1505 / 100 000EuropeValue and classValidated14675412[PMID]_17047148 [PMID]_32937680 [PMID]_36331704 [PMID]_37021783[PMID]
Point prevalenceUnknown—United KingdomClass onlyValidated14675412[PMID]_17047148 [PMID]_ORPHANET
Annual incidence1-9 / 100 0000.141 / 100 000United KingdomValue and classValidated14675412[PMID]_17047148 [PMID]_ORPHANET
Point prevalence1-9 / 1 000 0000.3063 / 100 000SpainValue and classValidated34521101[PMID]_ORPHANET
Annual incidence<1 / 1 000 0000.0829 / 100 000SpainValue and classValidated34521101[PMID]_ORPHANET
Point prevalenceUnknown—GermanyClass onlyValidated32937680[PMID]
Annual incidence1-9 / 1 000 0000.6 / 100 000GermanyValue and classValidated32937680[PMID]
Point prevalenceUnknown—AustraliaClass onlyValidated20169513[PMID]
Annual incidence1-9 / 1 000 0000.12 / 100 000AustraliaValue and classValidated20169513[PMID]
Point prevalenceUnknown—EuropeClass onlyValidated36331704[PMID]_ORPHANET
Point prevalenceUnknown—JapanClass onlyValidated28299631[PMID]_36331704[PMID]_ORPHANET
Annual incidence<1 / 1 000 0000.097 / 100 000JapanValue and classValidated28299631[PMID]_36331704[PMID]_ORPHANET
Point prevalenceUnknown—SwitzerlandClass onlyValidated37021783[PMID]
Annual incidence1-9 / 1 000 0000.45 / 100 000SwitzerlandValue and classValidated37021783[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