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127879008: Structure of parenchyma of liver (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
1166010 Hepatic parenchyma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474255013 Structure of parenchyma of liver en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
731812018 Structure of parenchyma of liver (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


37 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Structure of parenchyma of liver (body structure) Is a Liver part (body structure) true Inferred relationship Some
Structure of parenchyma of liver (body structure) Is a Organ parenchyma true Inferred relationship Some
Structure of parenchyma of liver (body structure) partie de Entire liver false Additional relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Entire parenchyma of liver Is a True Structure of parenchyma of liver (body structure) Inferred relationship Some
Hepatic parenchymal cell partie de False Structure of parenchyma of liver (body structure) Additional relationship Some
Intrahepatic haematoma Finding site False Structure of parenchyma of liver (body structure) Inferred relationship Some 1
Intrahepatic haematoma Finding site True Structure of parenchyma of liver (body structure) Inferred relationship Some 1
Associating liver partition and portal vein ligation for staged hepatectomy (procedure) Procedure site - Direct (attribute) True Structure of parenchyma of liver (body structure) Inferred relationship Some 3
Renal-hepatic-pancreatic dysplasia is a rare, genetic, developmental defect during embryogenesis syndrome characterized by the triad of pancreatic fibrosis (and cysts, with a reduction of parenchymal tissue), renal dysplasia (with peripheral cortical cysts, primitive collecting ducts, glomerular cysts and metaplastic cartilage) and hepatic dysgenesis (enlarged portal areas containing numerous elongated binary profiles with a tendency to perilobular fibrosis). Situs abnormalities, skeletal anomalies and anencephaly have also been associated. Patients that survive the neonatal period present renal insufficiency, chronic jaundice and insulin-dependent diabetes. Finding site True Structure of parenchyma of liver (body structure) Inferred relationship Some 3
A rare, genetic, parenchymal hepatic disease characterized by acute liver failure, that occurs in the first year of life, which manifests with failure to thrive, hypotonia, moderate global developmental delay, seizures, abnormal liver function tests, microcytic anemia and elevated serum lactate. Other associated features include hepatosteatosis and fibrosis, abnormal brain morphology, and renal tubulopathy. Minor illness exacerbates deterioration of liver failure. Finding site True Structure of parenchyma of liver (body structure) Inferred relationship Some 1
Hepatic lobule structure Is a True Structure of parenchyma of liver (body structure) Inferred relationship Some
A rare autosomal recessive axonal hereditary motor and sensory neuropathy characterized by infantile onset of recurrent episodes of acute liver failure (resulting in chronic liver fibrosis and hepatosplenomegaly), delayed motor development, cerebellar dysfunction presenting as gait disturbances and intention tremor, neurogenic stuttering, and motor and sensory neuropathy with muscle weakness especially in the lower legs, and numbness. Mild intellectual disability was reported in some patients. MRI of the brain shows non-progressive atrophy of the cerebellar vermis and thinning of the optic nerve. Finding site True Structure of parenchyma of liver (body structure) Inferred relationship Some 3
A rare genetic parenchymatous liver disease characterized by infantile or early childhood onset of recurrent episodes of acute liver failure precipitated by a febrile illness. During the life-threatening episodes, patients present with vomiting, lethargy, jaundice, as well as elevated levels of liver enzymes and coagulopathy. There is usually complete recovery between the episodes with conservative treatment. Finding site True Structure of parenchyma of liver (body structure) Inferred relationship Some 1

Reference Sets

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

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