aplasia cutis congenita of scalp 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. (Human Phenotype Ontology, HP_0007385)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007385
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5 genes associated with the aplasia cutis congenita of scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALX4 ALX homeobox 4
ARHGAP31 Rho GTPase activating protein 31
BMS1 BMS1 ribosome biogenesis factor
MSX2 msh homeobox 2
UBR1 ubiquitin protein ligase E3 component n-recognin 1