abnormality of the costochondral junction Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Any anomaly of the costochondral junction. The costochondral junctions 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_0000919)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0000919
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Genes

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

Symbol	Name
ALPL	alkaline phosphatase, liver/bone/kidney
CTNS	cystinosin, lysosomal cystine transporter
CYP27B1	cytochrome P450, family 27, subfamily B, polypeptide 1
CYP2R1	cytochrome P450, family 2, subfamily R, polypeptide 1
DDR2	discoidin domain receptor tyrosine kinase 2
DYM	dymeclin
FGFR3	fibroblast growth factor receptor 3
NOG	noggin
SBDS	Shwachman-Bodian-Diamond syndrome
SLC34A3	solute carrier family 34 (type II sodium/phosphate cotransporter), member 3
VDR	vitamin D (1,25- dihydroxyvitamin D3) receptor