Peroxisome biogenesis disorder 6B (DOID:0081435)
Alliance: disease page
Alt IDs: OMIM:614871
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 compound heterozygous mutation in the PEX10 gene on chromosome 1p36.