Term Name:	Peroxisome biogenesis disorder 7B
Synonyms:
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.
Ontology:	Human Disease [DOID:0081436]   ( DOID:0081436 )