|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Absence or underdevelopment of the urinary bladder. (Human Phenotype Ontology, HP_0010476)|
|Downloads & Tools|
1 genes associated with the aplasia/hypoplasia of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|MKS1||Meckel syndrome, type 1|