nuclear type mitochondrial complex I deficiency 12

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Summary

Literature (0)

DOID:0112099 - nuclear type mitochondrial complex I deficiency 12

Disease Ontology Definition:A nuclear type mitochondrial complex I deficiency that has_material_basis_in hemizygous mutation in the NDUFA1 gene on chromosome Xq24.

Synonyms: MC1DN12,

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): nuclear type mitochondrial complex I deficiency (is_a)