hypoplasia of the uterus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the uterus. (Human Phenotype Ontology, HP_0000013)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000013
Similar Terms
Downloads & Tools


10 genes associated with the hypoplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B3GALTL beta 1,3-galactosyltransferase-like
BMPR1B bone morphogenetic protein receptor, type IB
CLPP caseinolytic mitochondrial matrix peptidase proteolytic subunit
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
DCAF17 DDB1 and CUL4 associated factor 17
DHH desert hedgehog
HCCS holocytochrome c synthase
HNF1B HNF1 homeobox B
IRF6 interferon regulatory factor 6
STRA6 stimulated by retinoic acid 6