ORPHA:306644
Complication after organ transplantation
- 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 | Complication after organ transplantation | |
| fr | Complication après transplantation d'organe | |
| de | Komplikation nach Organtransplantation | |
| es | Complicaciones post-trasplante de órganos | |
| it | Complicazione in seguito a trapianto di organi | |
| nl | Complicatie na orgaantransplantatie | |
| pt | Complicação após transplante de órgão | |
| pl | Komplikacje po transplantacji narządów | |
| cs | Komplikace po orgánové transplantaci | |
| uk | Ускладнення після трансплантації органів | |
| zh | 器官移植术后并发症 | |
| tr | Organ nakli sonrası komplikasyon |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | T86.8 | BTNT | attributed | not yet validated |
| ICD-11 | NE84 | NTBT | attributed | validated |
| MONDO | 0700220 | E | validated | |
| MONDO | 700220 | E | validated | |
| UMLS | C5681087 | 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.
Codes that Orphanet moved or referred to this one:
- ORPHA:90055OBSOLETE: Rejection after corneal transplantation referred to · inactive
- ORPHA:91128OBSOLETE: Graft rejection after lung transplantation referred to · inactive
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 / 100 000 | 9 / 100 000 | Europe | Value and class | Validated | European Medicines Agency 2013[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/306644
- This record as JSON: /data/d/306644.json