FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term mitochondrial complex III deficiency ID (Ontology) DOID:0111139 (Human Disease)
Definition A mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial respiratory chain complex III.
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Human Disease Models (FBhh)  DOID       1
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 Human Disease Models
 mitochondrial complex III deficiency       1
Spanning Tree (Parents/Children)
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  inherited metabolic disorder
   |__mitochondrial metabolism disease
       |__mitochondrial complex III deficiency  17 rec.
           |__mitochondrial complex III deficiency nuclear type 1 4 rec.
           |__mitochondrial complex III deficiency nuclear type 2 4 rec.
           |__mitochondrial complex III deficiency nuclear type 3 2 rec.
           |__mitochondrial complex III deficiency nuclear type 4 1 rec.
           |__mitochondrial complex III deficiency nuclear type 5 1 rec.
           |__mitochondrial complex III deficiency nuclear type 6 2 rec.
           |__mitochondrial complex III deficiency nuclear type 7 1 rec.
           |__mitochondrial complex III deficiency nuclear type 8 1 rec.
           |__mitochondrial complex III deficiency nuclear type 9
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Is a mitochondrial metabolism disease
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Synonyms
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GARD:8295
MESH:C565128