| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores |
| 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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3 genes involed in the disease zellweger syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
