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Disease Ontology Browser
combined oxidative phosphorylation deficiency 15 (DOID:0111491)
Alliance: disease page
Synonyms: COXPD15
Alt IDs: OMIM:614947, ORDO:319524
Definition: A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation] in the MTFMT gene on chromosome 15q22.31.


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
07/05/2024
MGI 6.24
The Jackson Laboratory