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Disease Ontology Browser
nuclear type mitochondrial complex I deficiency 15 (DOID:0112077)
Alliance: disease page
Synonyms: MC1DN15
Alt IDs: OMIM:618237
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFAF4 on chromosome 6q16.1.


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
09/22/2022
MGI 6.21
The Jackson Laboratory