combined oxidative phosphorylation deficiency 40 Disease Ontology Browser

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combined oxidative phosphorylation deficiency 40 (DOID:0112117)
Alliance: disease page
Synonyms: COXPD40; QRSL1-related COXPD
Alt IDs: OMIM:618835, ORDO:570491
Definition: A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the QRSL1 gene on chromosome 6q21.

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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