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cytochrome C oxidase deficiency, fatal infantile, with cardioencephalomyopathy
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11451 |
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fatal infantile encephalocardiomyopathy caused by mutation in SCO2
|
11451 |
|
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SCO2 fatal infantile encephalocardiomyopathy
|
11451 |
|
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cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 1
|
11451 |
|
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cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1
|
11451 |
|
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cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1; CEMCOX1
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http://purl.obolibrary.org/obo/MONDO_0011451 |
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