ORPHA:599513
Acquired factor XIII deficiency
Synonyms: aFXIII
- 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| Lang | Name | Synonyms |
|---|---|---|
| en | Acquired factor XIII deficiency | aFXIII |
| fr | Déficit acquis en facteur XIII | |
| de | Faktor XIII-Mangel, erworbener | |
| es | Deficiencia del factor XIII adquirida | |
| it | Deficit acquisito del fattore XIII | = en |
| nl | Verworven deficiëntie van factor XIII | = en |
| pt | Deficiência de factor XIII adquirida | |
| pl | Nabyty niedobór czynnika XIII | = en |
| cs | Získaný deficit faktoru XIII | = en |
| uk | Набутий дефіцит фактора XIII | = en |
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 | 0021133 | E | validated | |
| UMLS | C0238120 | 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 |
|---|---|---|---|---|---|---|
| Cases/families | 95 cases | Worldwide | Case(s) | Validated | 30446212[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 30446212[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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/599513
- This record as JSON: /data/d/599513.json