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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Genes

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