|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormality of proteoglycan metabolism. (Human Phenotype Ontology, HP_0004355)|
|Downloads & Tools|
1 genes associated with the abnormality of proteoglycan metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|GNPTAB||N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits|