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Metadata
ID DOID:0080118
Name mitochondrial complex III deficiency nuclear type 9
Definition A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCC3 gene on chromosome 11q12.
http://omim.org/entry/616111?search=616111&highlight=616111
Xrefs

MIM:616111

Parent Relationships

is_a mitochondrial complex III deficiency

Subclass Logical Relationships

disease has basis in some structural_variant

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