|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Aplasia, that is failure to develop, of the ovary. (Human Phenotype Ontology, HP_0010463)|
|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.
|PTPN11||protein tyrosine phosphatase, non-receptor type 11|