fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 1 (Q60195355)
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fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in compound heterozygous mutation in the SCO2 gene on chromosome 22q13
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 1 |
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in compound heterozygous mutation in the SCO2 gene on chromosome 22q13 |
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1 reference