|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Atrophy of the cortex of the kidney. (Human Phenotype Ontology, HP_0002048)|
|Downloads & Tools|
1 genes associated with the renal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|MUC1||mucin 1, cell surface associated|