Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55670
Gene Symbol: PEX26
PEX26
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		0.510 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: 55670
Gene Symbol: PEX26
PEX26
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		0.510 Biomarker CTD_human Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation. 12851857

2003
Entrez Id: 55670
Gene Symbol: PEX26
PEX26
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		0.510 Biomarker GENOMICS_ENGLAND