Searched for "Cirrhosis".
31
results
found
on Genetics Home Reference.
Showing results 1 to 20.
- North American Indian childhood cirrhosis condition summary
Found: North American Indian childhood cirrhosis is a rare liver disorder that occurs...
- hypermanganesemia with dystonia, polycythemia, and cirrhosis condition summary
Found in name or synonym: hepatic cirrhosis, dystonia, polycythaemia, and hypermanganesaemia
- hemochromatosis condition summary
Found in name or synonym: Bronzed cirrhosis
- Alpers-Huttenlocher syndrome condition summary
Found in name or synonym: ...gray matter with hepatic cirrhosis
- cirrhosis definition
- alpha-1 antitrypsin deficiency condition summary
Found: ...develop liver damage (cirrhosis) due to the formation of scar tissue...
- African iron overload condition summary
Found: ...lead to chronic liver disease (cirrhosis) in people with African iron overload....
- cholesteryl ester storage disease condition summary
Found: ...chronic liver disease (cirrhosis) can develop. An accumulation...
- glycogen storage disease type III condition summary
Found: ...develop chronic liver disease (cirrhosis) and liver failure later in life....
- Berardinelli-Seip congenital lipodystrophy condition summary
- SLC30A10 gene summary
Official name: solute carrier family 30, member 10
Found: ...dystonia, polycythemia, and cirrhosis (HMDPC). This inherited disorder...
- congenital dyserythropoietic anemia condition summary
Found: ...and chronic liver disease (cirrhosis). Rarely, people with CDA type...
- glycogen storage disease type IV condition summary
Found: ...a form of liver disease called cirrhosis that often is irreversible. High...
- How are genetic conditions and genes named? in the Handbook
Found: ...dystonia, polycythemia, and cirrhosis);
- CIRH1A gene summary
Official name: cirrhosis, autosomal recessive 1A (cirhin)
Found: ...North American Indian childhood cirrhosis, a chronic liver disease identified...
- PHKG2 gene summary
Official name: phosphorylase kinase, gamma 2 (testis)
Found: ...as irreversible liver disease (cirrhosis). Mutations in the PHKG2 gene...
- familial hypobetalipoproteinemia condition summary
Found: ...to chronic liver disease (cirrhosis). Individuals with severe FHBL...
- X-linked sideroblastic anemia condition summary
Found: ...heart disease and liver damage (cirrhosis) can result from the buildup of...
- KRT18 gene information
Official name: keratin 18
Found: Cirrhosis (CIRRH) [MIM:215600]: A liver disease...
- KRT8 gene information
Official name: keratin 8
Found: Cirrhosis (CIRRH) [MIM:215600]: A liver disease...
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