aplasia/hypoplasia of the uterus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or developmental hypoplasia of the uterus. (Human Phenotype Ontology, HP_0008684)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008684
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13 genes associated with the aplasia/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
RBM8A RNA binding motif protein 8A
STRA6 stimulated by retinoic acid 6
WNT4 wingless-type MMTV integration site family, member 4
WNT7A wingless-type MMTV integration site family, member 7A