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Disease Ontology Browser
nuclear type mitochondrial complex I deficiency 3 (DOID:0112093)
Alliance: disease page
Synonyms: 'MC1DN3'
Alt IDs: OMIM:618224
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFS7 on chromosome 19p13.3.


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
06/23/2022
MGI 6.20
The Jackson Laboratory