Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5824
Gene Symbol: PEX19
PEX19
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome
0.500 Biomarker CTD_human Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly. 10051604

1999

Entrez Id: 5824
Gene Symbol: PEX19
PEX19
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome
0.500 Biomarker GENOMICS_ENGLAND