nuclear type mitochondrial complex I deficiency 30

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Summary

Literature (0)

DOID:0112098 - nuclear type mitochondrial complex I deficiency 30

Disease Ontology Definition:A nuclear type mitochondrial complex I deficiency that has_material_basis_in hemizygous mutation in the NDUFB11 gene on chromosome Xp11.3.

Synonyms: MC1DN30,

Xenbase 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: Alliance, 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)