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Disease Ontology Browser
mitochondrial complex III deficiency nuclear type 3 (DOID:0080112)
Alliance: disease page
Alt IDs: OMIM:615158
Definition: A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCRB gene on chromosome 8q22.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory