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Disease Ontology Browser
mitochondrial complex III deficiency nuclear type 9 (DOID:0080118)
Alliance: disease page
Alt IDs: OMIM:616111
Definition: A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCC3 gene on chromosome 11q12.

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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last database update
MGI 6.14
The Jackson Laboratory