cortical gyral simplification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal reduction of the number and complexity of the pattern of gyrations of the cerebral cortex. (Human Phenotype Ontology, HP_0009879)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009879
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Genes

3 genes associated with the cortical gyral simplification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
ERCC1 excision repair cross-complementation group 1
VLDLR very low density lipoprotein receptor