villous atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The enteric villi are atrophic or absent. (Human Phenotype Ontology, HP_0011473)
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14 genes associated with the villous atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
ALG3 ALG3, alpha-1,3- mannosyltransferase
CIITA class II, major histocompatibility complex, transactivator
EPCAM epithelial cell adhesion molecule
FOXP3 forkhead box P3
MPI mannose phosphate isomerase
MYO5B myosin VB
PCSK1 proprotein convertase subtilisin/kexin type 1
RFX5 regulatory factor X, 5 (influences HLA class II expression)
RFXANK regulatory factor X-associated ankyrin-containing protein
RFXAP regulatory factor X-associated protein
SKIV2L superkiller viralicidic activity 2-like (S. cerevisiae)
SPINK5 serine peptidase inhibitor, Kazal type 5
TTC37 tetratricopeptide repeat domain 37