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 |