ORPHA:599485
Acquired hemophilia B
Synonyms: AHB · Acquired F9 deficiency · Acquired factor IX deficiency
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult, Childhood, Elderly
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acquired hemophilia B | AHB · Acquired F9 deficiency · Acquired factor IX deficiency |
| fr | Hémophilie acquise B | Déficit acquis en F9 · Déficit acquis en facteur IX |
| de | Hämophilie B, erworbene | AHB · F9-Mangel, erworbener · Faktor IX-Mangel, erworbener |
| es | Hemofilia B adquirida | Deficiencia adquirida de F9 · Deficiencia adquirida de factor IX · HBA |
| it | Emofilia B acquisita | AHB · Deficit acquisito del fattore IX · Deficit acquisito di F9 |
| nl | Verworven hemofilie B | AHB · Verworven F9-deficiëntie · Verworven deficiëntie van factor IX |
| pt | Hemofilia B adquirida | Deficiência adquirida de F9 · Deficiência adquirida de factor IX · HBA |
| pl | Nabyta hemofilia B | AHB |
| cs | Získaná hemofilie B | = en |
| uk | Набута гемофілія В | Набута недостатність F9 · Набутий дефіцит фактора IX · AHB |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D68.4 | NTBT | attributed | validated |
| ICD-11 | 3B22 | NTBT | index | validated |
| MONDO | 0035736 | E | validated | |
| UMLS | C0398609 | E | validated | |
| MedDRA | 10082747 | E | validated |
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):
- ORPHA:166775Rare hemorrhagic disorder due to an acquired coagulation factor defect
rare hematological diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
| Annual incidence | Unknown | — | Worldwide | Class only | Validated | 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
- Orphanet page: orpha.net/en/disease/detail/599485
- This record as JSON: /data/d/599485.json