Peroxisome biogenesis disorder 7B (DOID:0081436)
Alliance: disease page
Alt IDs: OMIM:614873
Definition: A peroxisomal biogenesis disorder that is characterized by the overlapping phenotypes of neonatal adrenoleukodystrophy and infantile Refsum disease and that has_material_basis_in homozygous or compound heterozygous mutation in the PEX26 gene on chromosome 22q11.21.