Search Ontology:
Human Disease

mitochondrial complex III deficiency nuclear type 7

Term ID
DOID:0080116
Synonyms
Definition
A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCC2 gene on chromosome 6p21. http://omim.org/entry/615824?search=615824&highlight=615824
References
Ontology
Human Disease   ( DOID:0080116 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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