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Disease Ontology Browser
nuclear type mitochondrial complex I deficiency (DOID:0112065)
Alliance: disease page
Synonyms: MC1DN
Alt IDs: OMIM:PS252010
Definition: A mitochondrial complex I deficiency that has_material_basis_in mutation in a gene in the nuclear genome.

Disease References using Mouse Models (1)

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
12/10/2024
MGI 6.24
The Jackson Laboratory