Electron transfer flavoprotein-ubiquinone oxidoreductase defect
Symptom Information:
Symptom ID: | HPO:0003647 | ||
Synonyms: |
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Is a (Direct Parents): |
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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: |
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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) |