ORPHA:506222
Rare disorder potentially indicated for lung transplant
- Type
- Category
- Group
- Group of disorders
- Status
- active
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 lung transplant | |
| fr | Maladie rare possiblement indiquée pour la transplantation pulmonaire | |
| de | Seltene Erkrankung zur potentiellen Lungen-Transplantation indiziert | |
| es | Trastorno raro potencialmente indicado para trasplante pulmonar | |
| it | Malattia rara con indicazione al trapianto polmonare | |
| nl | Zeldzame aandoening mogelijk geïndiceerd voor longtransplantatie | |
| pt | Doença rara com potencial indicação para transplante pulmonar | |
| pl | Choroba rzadka będąca potencjalnym wskazaniem do przeszczepu płuc | |
| cs | Vzácná porucha indikovaná k transplantaci plic | |
| uk | Рідкісне захворювання, що є потенційним показанням для трансплантації легень | |
| zh | 可能适用于肺移植的罕见疾病 | |
| tr | Akciğer nakli için potansiyel olarak endike olan nadir hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681215 | 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:506207Rare disorder potentially indicated for transplant
rare transplant-related disorders
Children (7):
- ORPHA:1303Bronchiolitis obliterans
- ORPHA:137667Capillary malformation-arteriovenous malformation
- ORPHA:3188Congenital pulmonary veins atresia or stenosis
- ORPHA:586Cystic fibrosis
- ORPHA:182095Interstitial lung disease
- ORPHA:182090Pulmonary arterial hypertension
- ORPHA:692812RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome
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/506222
- This record as JSON: /data/d/506222.json