arthropathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A bone inflammation disease that is located_in joint. (Human Disease Ontology, DOID_381)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003040
Similar Terms
Downloads & Tools

Genes

10 genes associated with the arthropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANKH ANKH inorganic pyrophosphate transport regulator
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
COL11A1 collagen, type XI, alpha 1
COL2A1 collagen, type II, alpha 1
HFE hemochromatosis
HGD homogentisate 1,2-dioxygenase
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
MEFV Mediterranean fever
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PRG4 proteoglycan 4