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Metadata
ID	DOID:0081241
Name	peroxisome biogenesis disorder 3B
Definition	A peroxisome biogenesis disorder that has_material_basis_in homozygous or compound heterozygous mutation in the PEX12 gene on chromosome 17. https://pubmed.ncbi.nlm.nih.gov/22871920/
Xrefs	MIM:266510
Parent Relationships	is_a peroxisomal biogenesis disorder is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance