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Metadata
ID	DOID:0081439
Name	Peroxisome biogenesis disorder 11B
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 mutation in the PEX13 gene on chromosome 2p15. https://pubmed.ncbi.nlm.nih.gov/22871920/
Xrefs	MIM:614885
Parent Relationships	is_a peroxisomal biogenesis disorder is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance