Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Pituitary cyst |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
Cyst of septum pellucidum |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
Cyst of pineal gland (disorder) |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
Colloid cyst of third ventricle |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
Porencephalic cyst |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
Dermoid cyst of occipital lobe |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
A rare, nonprogressive, neurological disorder marked by intellectual deficit, spasticity and motor retardation associated with characteristic MRI findings of anterior bilateral temporal lobe cysts and multilobar leukoencephalopathy. So far, around 30 cases have been reported in the literature. Onset occurs in the first few months of life. Sensorineural deafness and microcephaly have also been reported. The etiology is unknown but an autosomal recessive mode of inheritance has been suggested. |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
Cystic leukoencephalopathy without megalencephaly is characterized by non-progressive leukoencephalopathy, bilateral cysts in the anterior part of the temporal lobe, cerebral white matter anomalies and severe psychomotor impairment. Less than 50 patients have been described in the literature so far. Inheritance is most likely autosomal recessive. |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
Infectious cyst of cerebral lobe |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
A rare genetic cerebral small vessel disease characterized by leukoencephalopathy and cerebral calcification and cysts due to diffuse cerebral microangiopathy resulting in microcystic and macrocystic parenchymal degeneration. The condition can present at any age from early childhood to late adulthood and manifests as a progressive cerebral degeneration. Symptoms are variable, but restricted to the central nervous systems, and include, among others, slowing of cognitive performance, seizures, and movement disorder with a combination of pyramidal, extrapyramidal, and cerebellar features. |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
Congenital cyst of cerebrum |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
Hydatid cyst of cerebrum (disorder) |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
Ependymal cyst of lateral ventricle of brain (disorder) |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
Cyst of basal ganglia (disorder) |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|
Interhemispheric cyst |
Is a |
True |
Cyst of cerebrum (disorder) |
Inferred relationship |
Some |
|