Search Ontology:
Human Disease
mitochondrial complex III deficiency nuclear type 7
- Term ID
- DOID:0080116
- Synonyms
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- 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 )
- is a type of
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