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Disease Ontology Browser
nuclear type mitochondrial complex I deficiency 2 (DOID:0112083)
Alliance: disease page
Synonyms: MC1DN2
Alt IDs: OMIM:618222
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFS8 on chromosome 11q13.2.

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