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Summary Literature (0)
DOID:0080622 - peroxisome biogenesis disorder 2B

Disease Ontology Definition:A peroxisomal biogenesis disorder that has_material_basis_in homozygous mutation in the PEX5 gene on chromosome 12p13.3.

Synonyms:

Xenbase Genes : pex10, pex26, pex1, pex5, pex13



Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a)