absence of pubertal development Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008197
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Genes

2 genes associated with the absence of pubertal development phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NR0B1 nuclear receptor subfamily 0, group B, member 1
TACR3 tachykinin receptor 3