ORPHA:506210
Rare disorder potentially indicated for liver 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 liver transplant | |
| fr | Maladie rare possiblement indiquée pour la transplantation hépatique | |
| de | Seltene Erkrankung zur potentiellen Leber-Transplantation indiziert | |
| es | Trastorno raro potencialmente indicado para trasplante hepático | |
| it | Malattia rara con indicazione al trapianto epatico | |
| nl | Zeldzame aandoening mogelijk geïndiceerd voor levertransplantatie | |
| pt | Doença rara com potencial indicação para transplante hepático | |
| pl | Choroba rzadka będąca potencjalnym wskazaniem do przeszczepu wątroby | |
| cs | Vzácná porucha indikovaná k transplantaci jater | |
| uk | Рідкісне захворювання, яке може бути показанням для трансплантації печінки | |
| zh | 可能适用于肝脏移植的罕见疾病 | |
| tr | Karaciğer nakli için potansiyel olarak endike olan nadir hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681218 | 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 (51):
- ORPHA:85443AL amyloidosis
- ORPHA:95157Acute hepatic porphyria
- ORPHA:52Alagille syndrome
- ORPHA:60Alpha-1-antitrypsin deficiency
- ORPHA:2137Autoimmune hepatitis
- ORPHA:300345Autosomal systemic lupus erythematosus
- ORPHA:163631Bile acid synthesis defect with cholestasis and malabsorption
- ORPHA:244283Biliary atresia with splenic malformation syndrome
- ORPHA:424982Biliary cystadenocarcinoma
- ORPHA:131Budd-Chiari syndrome
- ORPHA:53035Caroli disease
- ORPHA:480520Caroli syndrome
- ORPHA:70567Cholangiocarcinoma
- ORPHA:480501Choledochal cyst
- ORPHA:79239Classic galactosemia
- ORPHA:723101Clinical variant galactosemia
- ORPHA:529852Combined hepatocellular carcinoma and cholangiocarcinoma
- ORPHA:95507Congenital anomaly of hepatic vein
- ORPHA:480531Congenital portosystemic shunt
- ORPHA:205Crigler-Najjar syndrome
- ORPHA:586Cystic fibrosis
- ORPHA:401920Fibrolamellar hepatocellular carcinoma
- ORPHA:699068Fontan-associated liver disease
- ORPHA:35063Fulminant viral hepatitis
- ORPHA:364Glycogen storage disease due to glucose-6-phosphatase deficiency
- ORPHA:367Glycogen storage disease due to glycogen branching enzyme deficiency
- ORPHA:693846Hepatic arteriovenous malformation
- ORPHA:890Hepatic veno-occlusive disease
- ORPHA:449Hepatoblastoma
- ORPHA:88673Hepatocellular carcinoma
- ORPHA:271861Hereditary ATTR amyloidosis
- ORPHA:85450Hereditary amyloidosis with primary renal involvement
- ORPHA:469Hereditary fructose intolerance
- ORPHA:480512Idiopathic ductopenia
- ORPHA:30391Isolated biliary atresia
- ORPHA:485426Isolated congenital hepatic fibrosis
- ORPHA:2924Isolated polycystic liver disease
- ORPHA:389Langerhans cell histiocytosis
- ORPHA:566841Liver adenomatosis
- ORPHA:158061Macrophage activation syndrome
- ORPHA:446Neonatal hemochromatosis
- ORPHA:48372Nodular regenerative hyperplasia of the liver
- ORPHA:186Primary biliary cholangitis
- ORPHA:562639Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome
- ORPHA:100085Primary hepatic neuroendocrine carcinoma
- ORPHA:172Progressive familial intrahepatic cholestasis
- ORPHA:220489Rare hereditary hemochromatosis
- ORPHA:447771Sclerosing cholangitis
- ORPHA:882Tyrosinemia type 1
- ORPHA:330001Wild type ATTR amyloidosis
- ORPHA:905Wilson disease
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/506210
- This record as JSON: /data/d/506210.json