|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Lack of development of the glenoid fossa, also known as the glenoid cavity, which is the articular surface of the scapula that articulates with the head of the humerus. (Human Phenotype Ontology, HP_0006591)|
|Downloads & Tools|
1 genes associated with the absent glenoid fossa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|ORC1||origin recognition complex, subunit 1|