Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5193
Gene Symbol: PEX12
PEX12
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		0.530 Biomarker CTD_human Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalities. 26319495

2015
Entrez Id: 5193
Gene Symbol: PEX12
PEX12
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		0.530 Biomarker CTD_human Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders. 9090384

1997
Entrez Id: 5193
Gene Symbol: PEX12
PEX12
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		0.530 Biomarker GENOMICS_ENGLAND