aplasia/hypoplasia of the colon Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Congenital absence or underdevelopment of the colon. (Human Phenotype Ontology, HP_0100811)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100811
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4 genes associated with the aplasia/hypoplasia of the colon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTG2 actin, gamma 2, smooth muscle, enteric
GATA6 GATA binding protein 6
GUCY2C guanylate cyclase 2C
SOX10 SRY (sex determining region Y)-box 10