Schizencephaly Gene Set

Dataset ClinVar Gene-Phenotype 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
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Genes

1 genes associated with the Schizencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
COL4A1 collagen, type IV, alpha 1