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Disease Ontology Browser
peroxisome biogenesis disorder 3A (DOID:0080478)
Alliance: disease page
Synonyms: peroxisome biogenesis disorder 3A (Zellweger)
Alt IDs: OMIM:614859
Definition: A Zellweger syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PEX12 gene on chromosome 17.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory