combined oxidative phosphorylation deficiency 38 Disease Ontology Browser

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combined oxidative phosphorylation deficiency 38 (DOID:0111466)
Alliance: disease page
Synonyms: COXPD38
Alt IDs: OMIM:618378
Definition: A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MRPS14 gene on chromosome 1q25.1.

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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