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Metadata
ID	DOID:0080622
Name	peroxisome biogenesis disorder 2B
Definition	A peroxisomal biogenesis disorder that has_material_basis_in homozygous mutation in the PEX5 gene on chromosome 12p13.3. https://www.ncbi.nlm.nih.gov/pubmed/22871920
Xrefs	MIM:202370
Parent Relationships	is_a peroxisomal biogenesis disorder is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance