Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire parenchyma of brain (body structure) |
Is a |
True |
Structure of parenchyma of brain |
Inferred relationship |
Some |
|
A rare, neurodegenerative disease characterized by progressive cognitive impairment, spastic tetraparesis, and cerebellar ataxia resulting from amyloid deposits in the brain. Spasticity with increased deep tendon reflexes and tone are early symptoms, muscular rigidity evolves later. Progressive mental deterioration usually starts with apathy and impaired memory with progression to complete disorientation. |
Finding site |
True |
Structure of parenchyma of brain |
Inferred relationship |
Some |
4 |
A rare, neurodegenerative disease characterized by progressive dementia and ataxia, widespread cerebral amyloid angiopathy and parenchymal amyloid deposition. Two subtypes have been identified, ABri amyloidosis and ADan amyloidosis. |
Finding site |
True |
Structure of parenchyma of brain |
Inferred relationship |
Some |
2 |
A rare, neurodegenerative disease characterized by progressive cataracts, hearing loss, cerebellar ataxia, paranoid psychosis and dementia. Neuropathological features are diffuse atrophy of all parts of the brain, chronic diffuse encephalopathy and the presence of extremely thin and almost completely demyelinated cranial nerves. |
Finding site |
True |
Structure of parenchyma of brain |
Inferred relationship |
Some |
4 |
Injury of parenchyma of brain |
Finding site |
True |
Structure of parenchyma of brain |
Inferred relationship |
Some |
1 |
Intraparenchymal hematoma of brain (disorder) |
Finding site |
True |
Structure of parenchyma of brain |
Inferred relationship |
Some |
1 |
Intraparenchymal hemorrhage of brain (disorder) |
Finding site |
True |
Structure of parenchyma of brain |
Inferred relationship |
Some |
1 |
Bleeding into the tissue of the brain not due to a significant external force. Despite the word cerebral this includes all regions of brain tissue, not merely telencephalon. |
Finding site |
True |
Structure of parenchyma of brain |
Inferred relationship |
Some |
1 |
Traumatic intraparenchymal cerebral hemorrhage |
Finding site |
True |
Structure of parenchyma of brain |
Inferred relationship |
Some |
1 |
A rare multiple congenital anomalies/dysmorphic syndrome characterised by severe brain malformations associated with cerebral parenchymal underdevelopment, arthrogryposis and club feet due to mutations in KIAA1109 gene. Majority of the cases are early lethal. Milder cases may present with severe global developmental delay, intellectual disability, microcephaly, hydrocephaly, heart defects, renal problems, severe muscle hypotonia causing incapacity to stand without a support, epilepsy, syndactyly and variable dysmorphic facial features (including hypotelorism, hypertelorism, small eyes, low-set and posteriorly rotated ears, short nose, flattened nasal bridge, anteverted nares, retrognathia). |
Finding site |
True |
Structure of parenchyma of brain |
Inferred relationship |
Some |
1 |