Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Mumps hepatitis |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Chronic viral hepatitis B without delta-agent |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Hepatitis in coxsackie viral disease |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Viral hepatitis B without hepatic coma |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Chronic aggressive viral hepatitis |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Chronic active viral hepatitis |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Chronic persistent type B viral hepatitis (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Viral hepatitis, type A |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Viral hepatitis A without hepatic coma, without hepatitis delta (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Chronic active hepatitis C (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Coxsackie virus hepatitis |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Anicteric type A viral hepatitis |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Acute fulminating viral hepatitis |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Reactivation of hepatitis B viral hepatitis (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Cytomegalovirus hepatitis |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Chronic hepatitis C |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Chronic hepatitis E |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
hépatite non A, non B aiguë |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Acute hepatitis E |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Hepatic coma due to viral hepatitis C (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Hepatitis non-A non-B |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Relapsing type A viral hepatitis |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Acute type A viral hepatitis |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Acute type B viral hepatitis |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Posttransfusion viral hepatitis |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Acute fulminating type A viral hepatitis |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Acute fulminating type B viral hepatitis |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Acute alcoholic liver disease |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Specimen from liver obtained by partial lobectomy |
Specimen source topography |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Specimen from liver obtained by partial resection (specimen) |
Specimen source topography |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Acute hepatitis B with hepatitis D |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
3 |
hépatite aiguë B avec agent delta (co-infection) sans coma hépatique |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Chronic type B viral hepatitis |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Chronic viral hepatitis B with hepatitis D |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Chronic hepatitis C with stage 2 fibrosis |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Hepatic coma due to acute hepatitis B with delta agent (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Hepatitis B and hepatitis C |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Chronic viral hepatitis B without delta-agent |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Chronic persistent type B viral hepatitis (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Acute type B viral hepatitis |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Blastomycosis liver (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Chronic alcoholic liver disease (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Injury to liver during surgery |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Acute on chronic alcoholic liver disease (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Steatosis of liver caused by retroviral protease inhibitor |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Decompensated liver disease |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
|
Nodular regenerative hyperplasia of liver caused by antiretroviral drug (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Chronic hepatitis B with negative hepatitis B surface antigen and low level viral replication but positive hepatitis B virus deoxyribonucleic acid test. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Hepatic granuloma |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Nodular regenerative hyperplasia of liver |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Hepatic cystic hamartoma, also named mesenchymal hamartoma of liver, is a rare benign liver tumor of childhood, usually before the age of 2, of mesenchymal origin and variable clinical presentation (abdominal dissension, abdominal mass, pain, vomiting and signs of inferior vena cava compression). |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
A rare, severe complication occurring in the third trimester of pregnancy or in early postpartum period bearing a risk for perinatal and maternal mortality and characterized by jaundice, rise of hepatic injuries and evolving to acute liver failure and encephalopathy. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Reynolds syndrome (RS) is an autoimmune disorder characterized by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
5 |
Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterized by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harboring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Fine needle aspiration biopsy of liver using ultrasonographic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Fine needle aspiration biopsy of liver using ultrasonographic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
3 |
Wilson's disease |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Embryonal sarcoma of liver (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Primary hepatic neuroendocrine carcinoma (PHNEC) is a rare hepatic tumor that may manifest with abdominal pain or fullness, as well as diarrhea or weight loss. More than 10% of cases are asymptomatic and in rare cases a carcinoid syndrome may be observed. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Bile acid CoA ligase deficiency and defective amidation is an anomaly of bile acid synthesis characterized by fat malabsorption, neonatal cholestasis and growth failure. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
A mild subtype of citrin deficiency characterized clinically by low birth weight, failure to thrive, transient intrahepatic cholestasis, multiple aminoacidemia, galactosemia, hypoproteinemia, hepatomegaly, decreased coagulation factors, hemolytic anemia, variable but mostly mild liver dysfunction, and hypoglycemia. |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Percutaneous irreversible electroporation ablation of neoplasm of liver using computed tomography guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Percutaneous irreversible electroporation ablation of neoplasm of liver using computed tomography guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
3 |
A rare benign liver tumor characterized by a prominent inflammatory infiltrate and often mimicking a malignant liver neoplasm. The tumor is frequently solitary with a predilection for the right lobe; however, multiple lesions are possible. There are two clinicopathological subtypes: fibrohistiocytic inflammatory pseudotumor of the liver and lymphoplasmacytic inflammatory pseudotumor of the liver. Patients present with non-specific clinical symptoms such as abdominal pain or discomfort, fever, and weight loss. The condition may be associated with other chronic inflammatory or autoimmune diseases. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
A rare ciliopathy characterized by the association of nephronophthisis and liver fibrosis. Renal manifestations include chronic renal failure, polyuria, polydipsia, anemia, as well as increased echogenicity on renal ultrasound and interstitial fibrosis and tubular dilation on biopsy. Hepatic involvement manifests as hepatosplenomegaly with extensive fibrosis, destruction of the bile ducts, and cholestasis. Mild psychomotor retardation and ocular symptoms, such as strabismus, nystagmus, retinal degeneration, and anisocoria, have been reported in some patients. |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Decompensated cirrhosis of liver (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Viral arthritis co-occurrent with hepatitis |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterized by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harboring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining. |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
4 |
Bacterial hepatitis |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Ultrasonography of liver for early detection of hepatocellular carcinoma |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Congenital bile acid synthesis defect type 3 (BAS defect type 3) is a severe anomaly of bile acid synthesis characterized by severe neonatal cholestatic liver disease. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
A rare mitochondrial respiratory chain deficiency due to TRMU deficiency leading to mitochondrial tRNA synthesis defect and characterized clinically by transient, but life-threatening acute liver failure episodes. |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
A rare multiple congenital malformation syndrome, characterized by an association of cleft lip and palate, patchy pigmentary retinopathy (cat's paw), obstructive liver disease (cholestasis, portal hypertension etc.) and obstructive renal disease (ectopic ureteric insertion, obstruction, vesicoureteral reflux and hydronephrosis). Gastrointestinal tract involvement (malrotation, gastroesophageal reflux etc.) and cardiac involvement (coarctation of aorta, pulmonary artery stenosis, etc.) have also been reported. An overlap with Kabuki syndrome is debated. |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
7 |
Fibrosis of liver caused by alcohol (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Autoimmune hepatitis type 1 (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Autoimmune hepatitis type 2 (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Autoimmune hepatitis type 3 (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Ischemia reperfusion injury of liver (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Joubert syndrome with hepatic defect is a very rare subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with congenital hepatic fibrosis (CHF). |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Joubert syndrome with hepatic defect is a very rare subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with congenital hepatic fibrosis (CHF). |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Single photon emission computed tomography of liver (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Hepatitis caused by sexually transmissible virus (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Single photon emission computed tomography with computed tomography of liver (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Single photon emission computed tomography with computed tomography of liver (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
3 |
Injury of liver due to birth trauma (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Acute hepatic failure caused by hepatitis virus (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Subacute hepatic failure caused by hepatitis virus (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
The presence of metabolic dysfunction-associated steatotic liver disease (MASLD) in the absence of steatohepatitis. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Idiopathic granulomatous hepatitis (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Familial hypercholanemia is a very rare genetic disorder characterized clinically by elevated serum bile acid concentrations, itching, and fat malabsorption reported in patients of Old Order Amish descent. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Histoplasmosis liver |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Percutaneous needle biopsy of liver using computed tomography guidance (procedure) |
Procedure site - Indirect (attribute) |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Percutaneous needle biopsy of liver using computed tomography guidance (procedure) |
Procedure site - Direct (attribute) |
False |
Liver structure |
Inferred relationship |
Some |
3 |
A rare metabolic liver disease characterized by progressive liver disease and early cirrhosis due to accumulation of toxic cholesterol metabolites, which are detectable in bile, plasma, and urine, in association with dental abnormalities such as general hypomineralization and enamel hypoplasia, as well as occurrence of supernumerary teeth. There have been no further descriptions in the literature since 1996. |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
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. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
3 |
Magnetic resonance imaging of liver without contrast (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Retinohepatoendocrinologic syndrome (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
A genetically inherited anomaly of glycogen metabolism and a form of glycogen storage disease (GSD) characterized by fasting hypoglycemia. This is not a glycogenosis, strictly speaking, as the enzyme deficiency decreases glycogen reserves. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Glycogen storage disease due to muscle and heart glycogen synthase deficiency is characterized by muscle and heart glycogen deficiency. It has been described in three siblings (two brothers and their younger sister). The older brother died at 10.5 years of age as a result of sudden cardiac arrest and the younger brother presented with hypertrophic cardiomyopathy, abnormal heart rate and blood pressure during exercise, and muscle fatigability. The sister showed no symptoms but a lack of glycogen was identified through muscle biopsy. The syndrome is caused by homozygous missense mutations in the gene encoding muscle glycogen synthase. |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
4 |
Glycogen storage disease type IX (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |