absent glenoid fossa Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006591
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1 genes associated with the absent glenoid fossa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ORC1 origin recognition complex, subunit 1