nuclear type mitochondrial complex I deficiency 32 Disease Ontology Browser

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nuclear type mitochondrial complex I deficiency 32 (DOID:0112080)
Alliance: disease page
Synonyms: MC1DN32
Alt IDs: OMIM:618252
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFB8 gene on chromosome 10q24.31.

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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