aplasia cutis congenita over parietal area Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect resulting in the congenital absence of skin on the scalp in the parietal area. (Human Phenotype Ontology, HP_0004476)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004476
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1 genes associated with the aplasia cutis congenita over parietal area phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARHGAP31 Rho GTPase activating protein 31