Polymicrogyria
Disease ID: disease_node_13071
Connections displayed (default: 10).
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| Dbxref | MESH:D065706, NCI:C116936 |
|---|---|
| Subclassof | DOID_936 |
| Data Source | DOID, MESH |
| Mesh Id | D065706 |
| Mesh Label | Polymicrogyria |
| Mesh Subclassof | D065704 |
| Doid Label | polymicrogyria |
| Doid Description | A brain disease that is characterized by malformation of the developing brain characterized by abnormal cortical lamination and an unusual folding pattern of the cerebral cortex such that all or part of the brain surface is taken up by an excessive number of small folds (gyri). |
| Disease Node Id | disease_node_13071 |
| Doid Id | DOID_0080918 |
| Label | Polymicrogyria |
- Incoming r'ship
SUBCLASS_OFto/from Unilateral Focal Polymicrogyria(ID:disease_node_16163) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Brain Diseases(ID:disease_node_1682) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Bilateral Frontal Polymicrogyria(ID:disease_node_16158) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Bilateral Perisylvian Polymicrogyria(ID:disease_node_16159) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Bilateral Generalized Polymicrogyria(ID:disease_node_16162) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Bilateral Parasagittal Parieto-Occipital Polymicrogyria(ID:disease_node_16160) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Bilateral Frontoparietal Polymicrogyria(ID:disease_node_16161) (Disease)