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Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
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| Cytochrome-c Oxidase Deficiency | Legal notice |
Other terms
Cytochrome c Oxidase Deficiency,Cytochrome-c Oxidase Deficiencies,Deficiencies, Cytochrome-c Oxidase,Oxidase Deficiencies, Cytochrome-c,Oxidase Deficiency, Cytochrome-c,Cytochrome Oxidase Deficiency,Cytochrome Oxidase Deficiencies,Deficiencies, Cytochrome Oxidase,Deficiency, Cytochrome Oxidase,Oxidase Deficiencies, Cytochrome,Oxidase Deficiency, Cytochrome,Deficiency, Cytochrome-c Oxidase,Deficiency, Cytochrome c Oxidase
Description
Cytochrome-c Oxidase Deficiency: A disease that results from a congenital defect in ELECTRON TRANSPORT COMPLEX IV. Defects in ELECTRON TRANSPORT COMPLEX IV can be caused by mutations in the SURF1, SCO2, COX10, or SCO1 genes. ELECTRON TRANSPORT COMPLEX IV deficiency caused by mutation in SURF1 manifests itself as LEIGH DISEASE; that caused by mutation in SCO2 as fatal infantile cardioencephalomyopathy; that caused by mutation in COX10 as tubulopathy and leukodystrophy; and that caused by mutation in SCO1 as early-onset hepatic failure and neurologic disorder. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim, MIM#220110, May 17, 2001)
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