Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5194
Gene Symbol: PEX13
PEX13
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		0.310 Biomarker CTD_human Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations. 19449432

2009
Entrez Id: 5194
Gene Symbol: PEX13
PEX13
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		0.310 Biomarker CTD_human Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders. 10332040

1999