ORPHA:565779
Rare disorder potentially indicated for transplant or complication after transplantation
- Type
- Category
- Group
- Group of disorders
- Status
- active
- Flag
- Head of classification
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare disorder potentially indicated for transplant or complication after transplantation | |
| fr | Maladie rare possiblement indiquée pour une transplantation ou complication après transplantation | |
| de | Seltene Krankheit zur potentiellen Transplantation indiziert oder Komplikation nach Transplantation | |
| es | Trastorno raro potencialmente indicado para trasplante o complicaciones post-trasplante | |
| it | Malattia rara potenzialmente candidata al trapianto o a complicanze post-trapianto | |
| nl | Zeldzame aandoening mogelijk geïndiceerd voor transplantatie of complicatie na transplantatie | |
| pt | Doença rara potencialmente indicada para transplante ou complicação pós-transplante | |
| pl | Rzadkie zaburzenie potencjalnie wskazane do przeszczepu lub powikłań po przeszczepie | |
| cs | Vzácné onemocnění potenciálně indikované k transplantaci nebo při komplikaci po transplantaci | |
| uk | Рідкісне захворювання, що є потенційним показанням для трансплантації або ускладнення після трансплантації | |
| zh | 移植后可能出现的罕见疾病或并发症 | |
| tr | Organ nakli gerektirebilen nadir hastalık veya organ nakli sonrası görülen komplikasyonlar |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681283 | 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):
Children (9):
- ORPHA:306644Complication after organ transplantation
- ORPHA:90053Complications after hematopoietic stem cell transplantation
- ORPHA:244275De novo thrombotic microangiopathy after kidney transplantation
- ORPHA:39812Graft versus host disease
- ORPHA:90073Hepatitis B reinfection following liver transplantation
- ORPHA:633124Invasive scopulariopsis infection
- ORPHA:163921Posttransplant acute limbic encephalitis
- ORPHA:506207Rare disorder potentially indicated for transplant
- ORPHA:90052Recurrent hepatitis C virus induced liver disease in liver transplant recipients
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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/565779
- This record as JSON: /data/d/565779.json