peroxisome biogenesis disorder 14B (DOID:0081274)
Alliance: disease page
Alt IDs: OMIM:614920
Definition: A peroxisome biogenesis disorder that is characterized clinically by mild intellectual disability, congenital cataracts, progressive hearing loss, and polyneuropathy and that has_material_basis_in homozygous mutation in the PEX11B gene on chromosome 1q21.