|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Absence or underdevelopment of the choroid. (Human Phenotype Ontology, HP_0001122)|
|Downloads & Tools|
1 genes associated with the aplasia/hypoplasia of the choroid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|TRIM37||tripartite motif containing 37|