Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Glycogen phosphorylase kinase deficiency |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Glycogen phosphorylase kinase deficiency, X-linked |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Glycogen phosphorylase kinase deficiency, autosomal recessive |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cardiac glycogen phosphorylase kinase deficiency |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hepatic and muscle glycogen phosphorylase kinase deficiency |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hepatic glycogen phosphorylase kinase deficiency |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cirrhotic cardiomyopathy |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Percutaneous needle biopsy of liver using ultrasonographic guidance (procedure) |
Procedure site - Direct (attribute) |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Percutaneous needle biopsy of liver using ultrasonographic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Ataxia co-occurrent and due to cerebrotendinous xanthomatosis |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chorea co-occurrent and due to Wilson disease (disorder) |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Cirrhosis of liver caused by methotrexate |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Cirrhosis of liver caused by methotrexate |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Cirrhosis of liver caused by amiodarone |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Cirrhosis of liver caused by amiodarone |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Cirrhosis of liver caused by methyldopa (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Cirrhosis of liver caused by methyldopa (disorder) |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Hepatic ascites |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hepatic ascites due to chronic alcoholic hepatitis (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Liver disease co-occurrent and due to mitochondrial disorder (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cirrhosis of liver co-occurrent and due to primary sclerosing cholangitis (disorder) |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Neonatal haemorrhage of liver |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Traumatic rupture of liver (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic viral hepatitis D |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hypersensitivity disease of liver caused by drug (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Fibropolycystic disease of liver |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Fibropolycystic disease of liver |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Disorder of liver co-occurrent and due to disorder of urea cycle |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Disorder of liver due to disorder of mineral metabolism (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Partial nodular transformation of liver (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Percutaneous cryoablation of lesion of liver using computed tomography guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Percutaneous cryoablation of lesion of liver using computed tomography guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
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 (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
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 (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Hepatic pump technique (procedure) |
Procedure site - Indirect (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Disorder of liver due to disorder of amino acid metabolism (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Sickle cell hepatopathy |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Selective internal radiotherapy of liver using yttrium (90-Y) labeled microspheres |
Procedure site - Direct (attribute) |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Magnetic resonance imaging of liver and spleen with contrast (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
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 (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dynamic radionuclide imaging of liver using technetium (99m-Tc) (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dynamic radionuclide imaging of liver using radioisotope (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Radionuclide imaging of liver using radioactive isotope (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Static radionuclide imaging of liver using radioisotope |
Procedure site - Direct (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Radionuclide imaging of liver using rose bengal (131-I) sodium (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dynamic radionuclide imaging of liver and spleen using technetium (99m-Tc) (procedure) |
Procedure site - Direct (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Static radionuclide imaging of liver and spleen using technetium (99m-Tc) |
Procedure site - Direct (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Steatohepatitis caused by ingestible alcohol |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Steatohepatitis caused by ingestible alcohol |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Cholestasis of parenteral nutrition (disorder) |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Chronic lymphocytic cholangitis-cholangiohepatitis |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Deficiency of coagulation factor due to liver disease |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic hepatitis C caused by hepatitis C virus genotype 5 (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic hepatitis C caused by hepatitis C virus genotype 6 |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic hepatitis C caused by Hepatitis C virus genotype 2 |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic hepatitis C caused by Hepatitis C virus genotype 4 |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic hepatitis C caused by Hepatitis C virus genotype 1 |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic hepatitis C caused by Hepatitis C virus genotype 3 |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic hepatitis C caused by Hepatitis C virus genotype 1a (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic hepatitis C caused by Hepatitis C virus genotype 1b (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cirrhosis of liver co-occurrent and due to primary sclerosing cholangitis (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
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 (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cirrhosis of liver caused by methotrexate |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cirrhosis of liver caused by methyldopa (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cirrhosis of liver caused by amiodarone |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Portal cirrhosis (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Decompensated cirrhosis of liver (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Cirrhotic cardiomyopathy |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cirrhotic cardiomyopathy |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Cirrhosis of liver co-occurrent and due to primary sclerosing cholangitis (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A rare syndromic intellectual disability characterised 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, tachypnoea. There have been no further descriptions in the literature since 1987. |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Alcoholic liver damage |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Liver damage |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Alcoholic cirrhosis (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Acute on chronic alcoholic liver disease (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Alcoholic hepatic failure (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hepatocellular liver damage (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Zieve's syndrome (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic alcoholic liver disease (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hyperbiliverdinaemia |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Steroid dehydrogenase deficiency and dental anomaly syndrome (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic autoimmune hepatitis |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acute infectious hepatitis |
Finding site |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Acute infectious hepatitis |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Diagnostic laparoscopy of liver |
Procedure site - Direct (attribute) |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Diagnostic laparoscopy and biopsy of lesion of liver |
Procedure site - Direct (attribute) |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Diagnostic laparoscopy and biopsy of lesion of liver |
Procedure site - Direct (attribute) |
False |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Autoimmune hepatitis type 3 (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autoimmune hepatitis type 1 |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autoimmune hepatitis type 2 (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Contiguous ABCD1 DXS1357E deletion syndrome |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hepatomphalocele |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Transient infantile hypertriglyceridemia and hepatosteatosis |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Nephrocystin 3-related Meckel-like syndrome (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
MRI guided high intensity focused ultrasound ablation of lesion of liver |
Procedure site - Direct (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
MRI guided high intensity focused ultrasound ablation of lesion of liver |
Procedure site - Direct (attribute) |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Ferro-cerebro-cutaneous syndrome (disorder) |
Finding site |
True |
Liver structure (body structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |