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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
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

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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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