abdominal wall muscle weakness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Decreased strength of the abdominal musculature. (Human Phenotype Ontology, HP_0009023)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009023
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3 genes associated with the abdominal wall muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
SKI SKI proto-oncogene
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor