penoscrotal hypospadias Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A severe form of hypospadias in which the urethral opening is located at the junction of the penis and scrotum. (Human Phenotype Ontology, HP_0000808)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000808
Similar Terms
Downloads & Tools

Genes

1 genes associated with the penoscrotal hypospadias phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MAMLD1 mastermind-like domain containing 1