| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | The presence of a cleft in the cerebral cortex unilaterally or bilaterally, usually located in the frontal area. (Human Phenotype Ontology, HP_0010636) |
| External Link | http://www.omim.org/entry/269160 |
| Similar Terms | |
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3 genes associated with the schizencephaly phenotype from the curated OMIM Gene-Disease Associations dataset.
