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DeCS
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Descritor Inglês:
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Cytochrome-c Oxidase Deficiency
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Descritor Espanhol:
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Deficiencia de Citocromo-c Oxidasa
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Descritor Português:
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Deficiência de Citocromo-c Oxidase
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Sinônimos Inglês:
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Complex IV Deficiencies
Complex IV Deficiency
Cox Deficiencies
Cox Deficiency
Cytochrome C Oxidase Deficiency
Cytochrome Oxidase Deficiencies
Cytochrome Oxidase Deficiency
Cytochrome-c Oxidase Deficiencies
Deficiencies, Complex IV
Deficiencies, Cox
Deficiencies, Cytochrome Oxidase
Deficiencies, Cytochrome-c Oxidase
Deficiency, Complex IV
Deficiency, Cox
Deficiency, Cytochrome Oxidase
Deficiency, Cytochrome c Oxidase
Deficiency, Cytochrome-c Oxidase
Mitochondrial Complex IV Deficiency
Oxidase Deficiencies, Cytochrome
Oxidase Deficiencies, Cytochrome-c
Oxidase Deficiency, Cytochrome
Oxidase Deficiency, Cytochrome-c
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Categoria:
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C16.320.565.240
C18.452.660.195
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Definição Inglês:
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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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Relacionados Inglês:
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Electron Transport Complex IV
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Nota Histórica Inglês:
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2002
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Qualificadores Permitidos Inglês:
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Número do Registro:
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36031
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Identificador Único:
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D030401
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Ocorrência na BVS:
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Similar:
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DeCS
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