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Disease Ontology Browser
nuclear type mitochondrial complex I deficiency 23 (DOID:0112087)
Alliance: disease page
Synonyms: MC1DN23
Alt IDs: OMIM:618244
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA12 gene on chromosome 12q22.

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 6.22
The Jackson Laboratory