peroxisome biogenesis disorder due to PEX1 defect

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
peroxisome biogenesis disorder due to PEX1 defect
PEX1 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with peroxisome biogenesis disorder due to PEX1 defect.
5 View disease cluster →
Deafness enamel hypoplasia nail defects 1 shared genePEX1 Related via 1 shared gene including PEX1. Deafness-enamel hypoplasia-nail defects syndrome 1 shared genePEX1 Related via 1 shared gene including PEX1. Heimler syndrome 1 shared genePEX1 Related via 1 shared gene including PEX1. Peroxisomal disorder 1 shared genePEX1 Related via 1 shared gene including PEX1. Penile hypospadia 1 shared genePEX1 Related via 1 shared gene including PEX1.