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GTR Home > Conditions/Phenotypes > Mitochondrial complex III deficiency nuclear type 9

Mitochondrial complex III deficiency nuclear type 9

Summary

Any mitochondrial complex III deficiency in which the cause of the disease is a mutation in the UQCC3 gene. [from MONDO]

Available tests

10 tests are in the database for this condition.

Clinical tests (10 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: C11orf83, CCDS41658.1, MC3DN9, UNQ655, UQCC3
    Summary: ubiquinol-cytochrome c reductase complex assembly factor 3

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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