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mitochondrial complex IV deficiency nuclear type 1 (DOID:0070491)
Alliance: disease page
Synonyms: MC4DN1
Alt IDs: OMIM:220110, NCI:C176895, UMLS_CUI:C5435656
Definition: A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous or compound heterozygous mutation in the SURF1 gene on chromosome 9q34.2.

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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04/16/2024
MGI 6.23 		The Jackson Laboratory