Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0112065 - nuclear type mitochondrial complex I deficiency

Disease Ontology Definition:A mitochondrial complex I deficiency that has_material_basis_in mutation in a gene in the nuclear genome.

Synonyms: MC1DN

Xenbase Genes : ndufv1, ndufs4, ndufb9, ndufs1, ndufv2, nubpl, ndufb3, ndufs2, ndufaf5, ndufs3, ndufaf3, ndufa11, ndufaf1, ndufa1, ndufs6, [+]



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): mitochondrial complex I deficiency (is_a)