Cytochrome c oxidase deficiency
Symptom Information:
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Symptom ID:
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OMIM : No Id available
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Synonyms:
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Quality:
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Cross references:
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| OMIM: "Cytochrome c oxidase deficiency" [OMIM:Cytochrome c oxidase deficiency] |
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Is a (Direct Parents):
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Is a (Whole tree):
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HPO:
MedDRA:
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Database Frequency:
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2 / 7739
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Resource:
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All diseases associated with this symptom:
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Congenital lactic acidosis, Saguenay-Lac-St. Jean type
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(Orphanet:70472)
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Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
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(Orphanet:255235)
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