ORPHA:90053
Complications after hematopoietic stem cell transplantation
Synonyms: Complications after HSCT
- Type
- Particular clinical situation in a disease or syndrome
- 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
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Complications after hematopoietic stem cell transplantation | Complications after HSCT |
| fr | Complications après transplantation de cellules souches hématopoïétiques | |
| de | Komplikationen nach hämatopoetischer Stammzell-Transplantation | Komplikationen nach HSCT |
| es | Complicaciones post-trasplante de células madre hematopoyéticas | Complicaciones post-TCMH |
| it | Trapianto di cellule staminali ematopoietiche | |
| nl | Complicaties na hematopoëtische stamceltransplantatie | Complicaties na HSCT |
| pt | Transplantação de células hematopoiéticas | |
| pl | Transplantacja komórek hematopoetycznych | = en |
| cs | Transplantace krvetvorných kmenových buněk | = en |
| uk | Ускладнення після трансплантації гемопоетичних стовбурових клітин | Ускладнення після ТГСК |
| zh | 造血干细胞移植术后并发症 | HSCT后并发症 |
| tr | Hematopoetik kök hücre nakli sonrası komplikasyonlar | HSCT sonrası komplikasyonlar |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Z94.8 | NTBT | attributed | validated |
| ICD-11 | NE8Y | NTBT | attributed | validated |
| UMLS | C5680176 | 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):
- ORPHA:565779Rare disorder potentially indicated for transplant or complication after transplantation
Parents in the classifications (1):
- ORPHA:565779Rare disorder potentially indicated for transplant or complication after transplantation
rare transplant-related disorders
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-9 / 1 000 000 | 0.65 / 100 000 | Europe | Value and class | Validated | European Medicines Agency[OTHER] |
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/90053
- This record as JSON: /data/d/90053.json