Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Structure of superior occipital gyrus |
Is a |
True |
Structure of occipital lobe gyrus (body structure) |
Inferred relationship |
Some |
|
Entire occipital gyrus |
Is a |
False |
Structure of occipital lobe gyrus (body structure) |
Inferred relationship |
Some |
|
Structure of lateral occipital gyrus |
Is a |
True |
Structure of occipital lobe gyrus (body structure) |
Inferred relationship |
Some |
|
Structure of medial occipitotemporal gyrus |
Is a |
True |
Structure of occipital lobe gyrus (body structure) |
Inferred relationship |
Some |
|
Structure of lateral occipitotemporal gyrus |
Is a |
False |
Structure of occipital lobe gyrus (body structure) |
Inferred relationship |
Some |
|
Structure of lingual gyrus |
Is a |
True |
Structure of occipital lobe gyrus (body structure) |
Inferred relationship |
Some |
|
Structure of inferior occipital gyrus |
Is a |
True |
Structure of occipital lobe gyrus (body structure) |
Inferred relationship |
Some |
|
Entire occipital lobe gyrus (body structure) |
Is a |
True |
Structure of occipital lobe gyrus (body structure) |
Inferred relationship |
Some |
|
A rare genetic cerebral malformation characterized by the presence of cortical smoothening with loss of secondary and tertiary gyri, associated with an excessive number of small, irregular gyri with increased cortical thickness, located in the occipital lobes. Patients usually present with seizures (including myoclonic-astatic, absence, atypical absence, vision loss, myoclonic-atonic, generalized tonic-clonic) and variable (absent to moderate) developmental and/or intellectual delay. There is evidence the disease is caused by homozygous or compound heterozygous mutations in the LAMC3 gene on chromosome 9q34. |
Finding site |
True |
Structure of occipital lobe gyrus (body structure) |
Inferred relationship |
Some |
2 |
A rare genetic cerebral malformation characterized by the presence of cortical smoothening with loss of secondary and tertiary gyri, associated with an excessive number of small, irregular gyri with increased cortical thickness, located in the occipital lobes. Patients usually present with seizures (including myoclonic-astatic, absence, atypical absence, vision loss, myoclonic-atonic, generalized tonic-clonic) and variable (absent to moderate) developmental and/or intellectual delay. There is evidence the disease is caused by homozygous or compound heterozygous mutations in the LAMC3 gene on chromosome 9q34. |
Finding site |
True |
Structure of occipital lobe gyrus (body structure) |
Inferred relationship |
Some |
1 |
Bilateral parasagittal parieto-occipital polymicrogyria |
Finding site |
True |
Structure of occipital lobe gyrus (body structure) |
Inferred relationship |
Some |
2 |
Structure of occipital segment of fusiform gyrus |
Is a |
True |
Structure of occipital lobe gyrus (body structure) |
Inferred relationship |
Some |
|