abnormality of the sacroiliac joint Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the sacroiliac joint. (Human Phenotype Ontology, HP_0100781)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100781
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5 genes associated with the abnormality of the sacroiliac joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGFR3 fibroblast growth factor receptor 3
GPC3 glypican 3
SBDS Shwachman-Bodian-Diamond syndrome
SLC26A2 solute carrier family 26 (anion exchanger), member 2
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A