peroxisome biogenesis disorder 2A

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Summary

Literature (0)

DOID:0080477 - peroxisome biogenesis disorder 2A

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

Synonyms: peroxisome biogenesis disorder 2A (Zellweger),

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): peroxisomal biogenesis disorder (is_a)