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10200004: Liver structure (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
17776014 Liver en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
243351016 Liver structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
536442013 Liver structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
9011000077113 structure du foie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
117701000087113 foie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
920221000172112 hepar fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


309 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Liver structure Is a Liver and/or biliary structure (body structure) true Inferred relationship Some
Liver structure Is a Structure of abdominopelvic viscus false Inferred relationship Some
Liver structure Is a Digestive organ structure false Inferred relationship Some
Liver structure partie de Entire abdomen (body structure) false Additional relationship Some
Liver structure partie de Entire digestive system false Additional relationship Some
Liver structure partie de A large organ in the thorax, abdomen, or pelvis false Additional relationship Some
Liver structure Is a Structure of organ within abdomen proper cavity (body structure) true Inferred relationship Some

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

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

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