Electron transfer flavoprotein-ubiquinone oxidoreductase defect

Symptom Information:

Symptom ID: HPO:0003647
Synonyms:
Electron transfer flavoprotein-ubiquinone oxidoreductase defect [OMIM:Electron transfer flavoprotein-ubiquinone oxidoreductase defect]
Quality:
Cross references:
OMIM: "Electron transfer flavoprotein-ubiquinone oxidoreductase defect" [OMIM:Electron transfer flavoprotein-ubiquinone oxidoreductase defect]
Is a (Direct Parents):
HPO         Abnormality of mitochondrial metabolism
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of cell physiology(HPO:0011017)
             Abnormality of the mitochondrion(HPO:0012103)
                Abnormality of mitochondrial metabolism(HPO:0003287)
                   Electron transfer flavoprotein-ubiquinone oxidoreductase defect(HPO:0003647)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome (Orphanet:457185)