Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Chronic nonalcoholic liver disease |
Is a |
False |
Chronic liver disease |
Inferred relationship |
Some |
|
Other non-alcoholic chronic liver disease |
Is a |
False |
Chronic liver disease |
Inferred relationship |
Some |
|
Chronic liver disease NOS |
Is a |
False |
Chronic liver disease |
Inferred relationship |
Some |
|
Recurrent hepatitis |
Is a |
False |
Chronic liver disease |
Inferred relationship |
Some |
|
Hepatogenous chronic copper poisoning |
Is a |
False |
Chronic liver disease |
Inferred relationship |
Some |
|
Chronic hepatitis |
Is a |
True |
Chronic liver disease |
Inferred relationship |
Some |
|
Chronic passive congestion of liver |
Is a |
True |
Chronic liver disease |
Inferred relationship |
Some |
|
Benign recurrent intrahepatic cholestasis |
Is a |
False |
Chronic liver disease |
Inferred relationship |
Some |
|
Chronic nonalcoholic liver disease |
Is a |
True |
Chronic liver disease |
Inferred relationship |
Some |
|
Chronic yellow atrophy of liver |
Is a |
False |
Chronic liver disease |
Inferred relationship |
Some |
|
Local recurrence of malignant neoplasm of liver |
Is a |
False |
Chronic liver disease |
Inferred relationship |
Some |
|
Liver abscess and sequelae of chronic liver disease |
After |
True |
Chronic liver disease |
Inferred relationship |
Some |
2 |
Sequela of chronic liver disease (disorder) |
After |
True |
Chronic liver disease |
Inferred relationship |
Some |
1 |
Chronic alcoholic liver disease (disorder) |
Is a |
True |
Chronic liver disease |
Inferred relationship |
Some |
|
Chronic infection caused by Hepatitis D virus (disorder) |
Is a |
False |
Chronic liver disease |
Inferred relationship |
Some |
|
Cirrhosis of liver |
Is a |
True |
Chronic liver disease |
Inferred relationship |
Some |
|
Chronic rejection of liver transplant (disorder) |
Is a |
True |
Chronic liver disease |
Inferred relationship |
Some |
|
Relapsing viral hepatitis |
Is a |
False |
Chronic liver disease |
Inferred relationship |
Some |
|
Chronic necrosis of liver |
Is a |
True |
Chronic liver disease |
Inferred relationship |
Some |
|
A rare disease, manifesting with idiopathic pulmonary fibrosis, hepatic nodular regenerative hyperplasia leading to portal hypertension and thrombocytopenia due to bone marrow hypoplasia. The condition was associated with 100% mortality. |
Is a |
True |
Chronic liver disease |
Inferred relationship |
Some |
|
Progressive familial intrahepatic cholestasis (PFIC) refers to a heterogeneous group of autosomal recessive disorders of childhood that disrupt bile formation and present with cholestasis of hepatocellular origin. |
Is a |
True |
Chronic liver disease |
Inferred relationship |
Some |
|
Chronic hepatic failure |
Is a |
True |
Chronic liver disease |
Inferred relationship |
Some |
|
Autoantibody negative autoimmune hepatitis |
Is a |
True |
Chronic liver disease |
Inferred relationship |
Some |
|
A rare genetic parenchymatous liver disease characterized by infantile or early childhood onset of recurrent episodes of acute liver failure precipitated by a febrile illness. During the life-threatening episodes, patients present with vomiting, lethargy, jaundice, as well as elevated levels of liver enzymes and coagulopathy. There is usually complete recovery between the episodes with conservative treatment. |
Is a |
False |
Chronic liver disease |
Inferred relationship |
Some |
|
A rare biliary tract disease characterized by loss of interlobular bile ducts resulting in chronic cholestasis, without any known cause. Loss of less than 50% of interlobular bile ducts is associated with a mild disease course, while loss of the majority of ducts results in a severe form, potentially leading to cirrhosis and liver failure. Patients typically present as young or middle-aged adults with episodic jaundice, pruritus, and elevated liver enzymes. |
Is a |
True |
Chronic liver disease |
Inferred relationship |
Some |
|