| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores 2025 |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A congenital abnormality of the cerebral hemisphere characterized by an excessive number of small gyri (convolutions) on the surface of the brain. (Human Phenotype Ontology, HP_0002126) |
| Similar Terms | |
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2 genes involed in the disease Polymicrogyria from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
