(Q60195358)

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fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 3

fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in homozygous mutation in the COA5 gene on chromosome 2q11

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autosomal recessive disease

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30 November 2020

fatal infantile encephalocardiomyopathy

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30 November 2020

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WikiProject Medicine

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http://purl.obolibrary.org/obo/DOID_0080359

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30 November 2020

http://identifiers.org/doid/DOID:0080359

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30 November 2020

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28 August 2019

(Q60195358)

fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 3

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