aplasia of the ovary Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Aplasia, that is failure to develop, of the ovary. (Human Phenotype Ontology, HP_0010463)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010463
Similar Terms
Downloads & Tools


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

Symbol Name
PTPN11 protein tyrosine phosphatase, non-receptor type 11