abnormality of the glenoid fossa Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly 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_0011912)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011912
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Genes

4 genes associated with the abnormality of the glenoid fossa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DYM dymeclin
LMX1B LIM homeobox transcription factor 1, beta
ORC1 origin recognition complex, subunit 1
SCARF2 scavenger receptor class F, member 2