enlargement of the costochondral junction Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormally increased size of the costochondral junctions, which are located between the distal part of the ribs and the costal cartilages, which are bars of hyaline cartilage that connect the ribs to the sternum. (Human Phenotype Ontology, HP_0000920)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000920
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Genes

6 genes associated with the enlargement of the costochondral junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
CYP2R1 cytochrome P450, family 2, subfamily R, polypeptide 1
DYM dymeclin
NOG noggin
SBDS Shwachman-Bodian-Diamond syndrome
SLC34A3 solute carrier family 34 (type II sodium/phosphate cotransporter), member 3