Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Glycogen storage disease type IX (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Glycogen phosphorylase kinase deficiency, X-linked |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
1 |
Glycogen phosphorylase kinase deficiency, autosomal recessive |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Cardiac glycogen phosphorylase kinase deficiency |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Hepatic and muscle glycogen phosphorylase kinase deficiency |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Hepatic glycogen phosphorylase kinase deficiency |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Cirrhotic cardiomyopathy is the term used to describe a constellation of features indicative of abnormal heart structure and function in patients with cirrhosis. These include systolic and diastolic dysfunction, electrophysiological changes, and macroscopic and microscopic structural changes. |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
4 |
Percutaneous needle biopsy of liver using ultrasonographic guidance (procedure) |
Procedure site - Direct (attribute) |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Percutaneous needle biopsy of liver using ultrasonographic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
3 |
Ataxia co-occurrent and due to cerebrotendinous xanthomatosis |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
1 |
Chorea co-occurrent and due to Wilson disease (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
6 |
Cirrhosis of liver caused by methotrexate (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Cirrhosis of liver caused by methotrexate (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Cirrhosis of liver caused by amiodarone (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Cirrhosis of liver caused by amiodarone (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Cirrhosis of liver caused by methyldopa (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Cirrhosis of liver caused by methyldopa (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
3 |
Hepatic ascites |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Hepatic ascites due to chronic alcoholic hepatitis (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
3 |
Liver disease co-occurrent and due to mitochondrial disorder (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Cirrhosis of liver co-occurrent and due to primary sclerosing cholangitis (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
4 |
Neonatal hemorrhage of liver (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Traumatic rupture of liver (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Chronic infection caused by Hepatitis D virus (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Hypersensitivity disease of liver caused by drug (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Fibropolycystic disease of liver |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Fibropolycystic disease of liver |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
3 |
Disorder of liver co-occurrent and due to disorder of urea cycle (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Disorder of liver due to disorder of mineral metabolism (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Partial nodular transformation of liver |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Percutaneous cryoablation of lesion of liver using computed tomography guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Percutaneous cryoablation of lesion of liver using computed tomography guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
3 |
Single photon emission computed tomography with computed tomography of liver using technetium Tc^99m^ sulfur colloid (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Single photon emission computed tomography with computed tomography of liver using technetium Tc^99m^ sulfur colloid (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
3 |
Rhythmic compression applied over the liver for purposes of increasing blood flow through the liver and enhancing bile and lymphatic drainage from the liver. |
Procedure site - Indirect (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Disorder of liver due to disorder of amino acid metabolism (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Disorder of liver due to sickle cell disease (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Selective internal radiotherapy of liver using yttrium (90-Y) labeled microspheres |
Procedure site - Direct (attribute) |
False |
Liver structure |
Inferred relationship |
Some |
1 |
Magnetic resonance imaging of liver and spleen with contrast (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
2 |
A rare, inherited mitochondrial disorder due to a defect in mitochondrial protein synthesis characterized by intrauterine growth retardation, metabolic decompensation with recurrent vomiting, persistent severe lactic acidosis, encephalopathy, seizures, failure to thrive, severe global developmental delay, poor eye contact, severe muscular hypotonia or axial hypotonia with limb hypertonia, hepatomegaly and/or liver dysfunction and/or liver failure, leading to fatal outcome in severe cases. Neuroimaging abnormalities may include corpus callosum thinning, leukodystrophy, delayed myelination and basal ganglia involvement. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Dynamic radionuclide imaging of liver using technetium (99m-Tc) (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Dynamic radionuclide imaging of liver using radioisotope (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Radionuclide imaging of liver using radioactive isotope (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Static radionuclide imaging of liver using radioisotope |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Radionuclide imaging of liver using rose bengal (131-I) sodium (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Dynamic radionuclide imaging of liver and spleen using technetium (99m-Tc) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Static radionuclide imaging of liver and spleen using technetium (99m-Tc) |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Steatohepatitis caused by ingestible alcohol |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
1 |
Steatohepatitis caused by ingestible alcohol |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Cholestasis of parenteral nutrition (disorder) |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Chronic lymphocytic cholangitis-cholangiohepatitis |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Deficiency of coagulation factor due to liver disease |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Chronic hepatitis C caused by hepatitis C virus genotype 5 (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Chronic hepatitis C caused by hepatitis C virus genotype 6 (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Chronic hepatitis C caused by Hepatitis C virus genotype 2 |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Chronic hepatitis C caused by Hepatitis C virus genotype 4 |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Chronic hepatitis C caused by Hepatitis C virus genotype 1 (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Chronic hepatitis C caused by Hepatitis C virus genotype 3 |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Chronic hepatitis C caused by Hepatitis C virus genotype 1a (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Chronic hepatitis C caused by Hepatitis C virus genotype 1b (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Cirrhosis of liver co-occurrent and due to primary sclerosing cholangitis (disorder) |
Finding site |
True |
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 |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Cirrhosis of liver caused by methotrexate (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Cirrhosis of liver caused by methyldopa (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Cirrhosis of liver caused by amiodarone (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Portal cirrhosis (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Decompensated cirrhosis of liver (disorder) |
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 |
1 |
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 |
2 |
Cirrhotic cardiomyopathy is the term used to describe a constellation of features indicative of abnormal heart structure and function in patients with cirrhosis. These include systolic and diastolic dysfunction, electrophysiological changes, and macroscopic and microscopic structural changes. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Cirrhotic cardiomyopathy is the term used to describe a constellation of features indicative of abnormal heart structure and function in patients with cirrhosis. These include systolic and diastolic dysfunction, electrophysiological changes, and macroscopic and microscopic structural changes. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Cirrhosis of liver co-occurrent and due to primary sclerosing cholangitis (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Hepatic fibrosis-renal cysts-intellectual disability syndrome is a rare, syndromic intellectual disability characterized by early developmental delay with failure to thrive, intellectual disability, congenital hepatic fibrosis, renal cystic dysplasia, and dysmorphic facial features (bilateral ptosis, anteverted nostrils, high arched palate, and micrognathia). Variable additional features have been reported, including cerebellar anomalies, postaxial polydactyly, syndactyly, genital anomalies, tachypnea. There have been no further descriptions in the literature since 1987. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
3 |
Alcoholic liver damage (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Liver damage |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Alcoholic cirrhosis (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
3 |
Acute on chronic alcoholic liver disease (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Alcoholic hepatic failure |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Hepatocellular liver damage (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Zieve's syndrome |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Chronic alcoholic liver disease (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Hyperbiliverdinemia is a rare, genetic hepatic disease characterized by the presence of green coloration of the skin, urine, plasma and other body fluids (ascites, breastmilk) or parts (sclerae) due to increased serum levels of biliverdin in association with biliary obstruction and/or liver failure. Association with malnutrition, medication, and congenital biliary atresia has also been reported. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
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 |
True |
Liver structure |
Inferred relationship |
Some |
1 |
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 |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Chronic autoimmune hepatitis |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Acute infectious hepatitis |
Finding site |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Acute infectious hepatitis |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Diagnostic laparoscopy of liver |
Procedure site - Direct (attribute) |
False |
Liver structure |
Inferred relationship |
Some |
1 |
Diagnostic laparoscopy and biopsy of lesion of liver |
Procedure site - Direct (attribute) |
False |
Liver structure |
Inferred relationship |
Some |
1 |
Diagnostic laparoscopy and biopsy of lesion of liver |
Procedure site - Direct (attribute) |
False |
Liver structure |
Inferred relationship |
Some |
2 |
Autoimmune hepatitis type 3 (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Autoimmune hepatitis type 1 (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
Autoimmune hepatitis type 2 (disorder) |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
1 |
CADDS is a rare, genetic, neurometabolic disease characterized by severe intrauterine growth retardation, failure to thrive, profound neonatal hypotonia, severe global development delay, elevated very long chain fatty acids in plasma, and neonatal cholestasis leading to hepatic failure and death. Other features include ocular abnormalities (e.g. blindness and cataracts), sensorineural deafness, seizures, and abnormal brain morphology (notably delayed CNS myelination and ventriculomegaly). |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Hepatomphalocele |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Transient infantile hypertriglyceridemia and hepatosteatosis is a rare, genetic, hepatic disease characterized by massive hepatomegaly, moderate to severe, transient hypertriglyceridemia and hepatic steatosis (followed by fibrosis), manifesting in infancy with failure to thrive, vomiting, an enlarged abdomen and a fatty liver. Reduction or normalization of triglyceride serum levels occurs with advancing age. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
A rare sterol metabolism disorder characterized by increased LDL cholesterol serum levels (which are resistant to treatment with 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors), hypertriglyceridemia, and decreased rate of bile acid excretion, resulting from cholesterol 7alpha-hydroxylase deficiency. Premature gallstone disease and/or premature coronary and peripheral vascular disease are frequently associated. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
2 |
NPHP3-related Meckel-like syndrome is a rare, genetic, syndromic renal malformation characterized by cystic renal dysplasia with or without prenatal oligohydramnios, central nervous system abnormalities (commonly Dandy-Walker malformation), congenital hepatic fibrosis, and absence of polydactyly. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
3 |
MRI guided high intensity focused ultrasound ablation of lesion of liver |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
1 |
MRI guided high intensity focused ultrasound ablation of lesion of liver |
Procedure site - Direct (attribute) |
True |
Liver structure |
Inferred relationship |
Some |
2 |
Ferro-cerebro-cutaneous syndrome is a rare, genetic, metabolic liver disease characterized by progressive neurodegeneration, cutaneous abnormalities, including varying degrees of ichthyosis or seborrheic dermatitis, and systemic iron overload. Patients manifest with infantile-onset seizures, encephalopathy, abnormal eye movements, axial hypotonia with peripheral hypertonia, brisk reflexes, cortical blindness and deafness, myoclonus and hepato/splenomegaly, as well as oral manifestations, including microdontia, widely spaced and pointed teeth with delayed eruption, and gingival overgrowth. |
Finding site |
True |
Liver structure |
Inferred relationship |
Some |
3 |