dysostosis multiplex Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000943
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Genes

16 genes associated with the dysostosis multiplex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGA aspartylglucosaminidase
ARSB arylsulfatase B
CTSA cathepsin A
FUCA1 fucosidase, alpha-L- 1, tissue
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GNPTG N-acetylglucosamine-1-phosphate transferase, gamma subunit
GNS glucosamine (N-acetyl)-6-sulfatase
GUSB glucuronidase, beta
HGSNAT heparan-alpha-glucosaminide N-acetyltransferase
IDS iduronate 2-sulfatase
IDUA iduronidase, alpha-L-
MAN2B1 mannosidase, alpha, class 2B, member 1
NAGLU N-acetylglucosaminidase, alpha
NEU1 sialidase 1 (lysosomal sialidase)
SGSH N-sulfoglucosamine sulfohydrolase
SUMF1 sulfatase modifying factor 1