aplasia cutis congenita on trunk or limbs 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 trunk or the limbs. (Human Phenotype Ontology, HP_0007589)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007589
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1 genes associated with the aplasia cutis congenita on trunk or limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARHGAP31 Rho GTPase activating protein 31