| Dataset | HPO 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://compbio.charite.de/hpoweb/showterm?id=HP:0010636 |
| Similar Terms | |
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3 genes associated with the schizencephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
