Search Ontology:
Human Disease

mitochondrial complex III deficiency nuclear type 4

Term ID
DOID:0080113
Synonyms
Definition
A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCRQ gene on chromosome 5q31. http://omim.org/entry/615159?search=615159&highlight=615159
References
Ontology
Human Disease   ( DOID:0080113 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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