bilateral cryptorchidism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of both testes from the scrotum owing to failure of the testis or testes to descend through the inguinal canal to the testis. (Human Phenotype Ontology, HP_0008689)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008689
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Genes

4 genes associated with the bilateral cryptorchidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMH anti-Mullerian hormone
AMHR2 anti-Mullerian hormone receptor, type II
RIPK4 receptor-interacting serine-threonine kinase 4
ZBTB20 zinc finger and BTB domain containing 20