mitochondrial complex III deficiency nuclear type 7 Disease Ontology Browser

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Disease Ontology Browser

mitochondrial complex III deficiency nuclear type 7 (DOID:0080116)
Alliance: disease page
Alt IDs: OMIM:615824
Definition: A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCC2 gene on chromosome 6p21.

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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