peroxisome-biogenesis disorder Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A peroxisomal disease that is characterized by the reduction or absence of functional peroxisomes in the cells of an individual that has_material_basis_in autosomal recessive inheritance of a mutation in the peroxisome biogenesis factor (PEX) genes. (Human Disease Ontology, DOID_905)
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Genes

1 genes associated with the disease peroxisome-biogenesis disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
PEX26 peroxisomal biogenesis factor 26