mitochondrial complex V (ATP synthase) deficiency nuclear type 7 Disease Ontology Browser

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Disease Ontology Browser

mitochondrial complex V (ATP synthase) deficiency nuclear type 7 (DOID:0070464)
Alliance: disease page
Synonyms: MC5DN7
Alt IDs: OMIM:620359
Definition: A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the ATP5PO gene on chromosome 21q22.11.

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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