Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Partial epileptic seizure of occipital lobe with impairment of consciousness |
Finding site |
False |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Self-limited epilepsy with autonomic seizures |
Finding site |
False |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Benign occipital epilepsy is a rare, genetic neurological disorder characterised by visual seizures and occipital epileptiform paroxysms reactive to ocular opening which present in infancy to mid-adolescence. Vomiting, tonic eye deviation and impairment of consciousness are typically associated with the Panayiotopoulos type, while visual hallucinations, ictal blindness and post-ictal headache are commonly observed in the Gastaut type. Electroencephalographic findings in both types are similar and include bilateral, synchronous, high voltage spike-wave complexes in a normal background activity located predominantly in the occipital lobes. |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Childhood occipital visual epilepsy (disorder) |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Retinal detachment and occipital encephalocele |
Finding site |
False |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Retinal detachment and occipital encephalocele |
Finding site |
False |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Zechi Ceide syndrome |
Finding site |
False |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare genetic bone development disorder characterized by occipital and parietal bone hypoplasia leading to occipital encephalocele, calvarial mineralization defects, craniosynostosis, radiohumeral fusions, oligodactyly and other skeletal anomalies (arachnodactyly, terminal phalangeal aplasia of the thumbs, bilateral absence of the great toes, pronounced bilateral angulation of femora, shortened limbs, advanced osseous maturation). Fetal death in utero is associated. There is evidence the disease can be caused by homozygous mutation in the CYP26B1 gene on chromosome 2p13. |
Finding site |
False |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Zechi Ceide syndrome |
Finding site |
False |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Occipital encephalocele |
Finding site |
False |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Focal contusion of occipital lobe (disorder) |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dermoid cyst of occipital lobe |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Abscess of occipital lobe |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A rare genetic bone development disorder characterized by occipital and parietal bone hypoplasia leading to occipital encephalocele, calvarial mineralization defects, craniosynostosis, radiohumeral fusions, oligodactyly and other skeletal anomalies (arachnodactyly, terminal phalangeal aplasia of the thumbs, bilateral absence of the great toes, pronounced bilateral angulation of femora, shortened limbs, advanced osseous maturation). Fetal death in utero is associated. There is evidence the disease can be caused by homozygous mutation in the CYP26B1 gene on chromosome 2p13. |
Finding site |
False |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Focal contusion of occipital lobe (disorder) |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Primary glioblastoma multiforme of occipital lobe |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary anaplastic astrocytoma of occipital lobe (disorder) |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary malignant glioma of occipital lobe (disorder) |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary astrocytoma of occipital lobe (disorder) |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary oligodendroglioma of occipital lobe |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
An epileptic seizure originating within unilateral networks limited to the occipital lobe. Seizures arising in the occipital lobe are characterized by subjective visual phenomenon and/or oculomotor features such as forced eye closure, eyelid fluttering, eye deviation and nystagmus. |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary malignant ependymoma of occipital lobe |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Photosensitive occipital lobe epilepsy |
Finding site |
True |
Occipital lobe structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |