Search Ontology:
Human Disease

mitochondrial complex III deficiency nuclear type 9

Term ID
DOID:0080118
Synonyms
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
References
Ontology
Human Disease   ( DOID:0080118 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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