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Disease Ontology Browser
combined oxidative phosphorylation deficiency 25 (DOID:0111468)
Alliance: disease page
Synonyms: COXPD25
Alt IDs: OMIM:616430, ORDO:447954
Definition: A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in MARS2 on chromosome 2q33.1.


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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last database update
01/31/2023
MGI 6.22
The Jackson Laboratory