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Standards Ontologies Notations
mitochondrial complex III deficiency nuclear type 9

Summary
Definition
A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCC3 gene on chromosome 11q12.
Super Class
mitochondrial complex III deficiency
Disease Ontology
DOID:0080118
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
790955 UQCC3 ubiquinol-cytochrome c reductase complex assembly factor 3
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024