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Summary Literature (0)
DOID:0081241 - peroxisome biogenesis disorder 3B

Disease Ontology Definition:A peroxisome biogenesis disorder that has_material_basis_in homozygous or compound heterozygous mutation in the PEX12 gene on chromosome 17.

Synonyms:

Xenbase Genes : pex26, pex1, pex12, pex2



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

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