glenoid fossa hypoplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the glenoid fossa, which is the cavity in the lateral part of the scapula which articulates with the head of the humerus. (Human Phenotype Ontology, HP_0006633)
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2 genes associated with the glenoid fossa hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
LMX1B LIM homeobox transcription factor 1, beta
SCARF2 scavenger receptor class F, member 2