5C53.21 Multiple mitochondrial DNA deletion syndromes

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

This is the multiple DNA located in organelles called mitochondria, structures within eukaryotic cells that convert the chemical energy from food into a form that cells can use, adenosine triphosphate (ATP).

code elsewhere

• Progressive external ophthalmoplegia, autosomal dominant  (9C82.0)
• Progressive external ophthalmoplegia, autosomal recessive  (9C82.0)
• Autosomal dominant optic atrophy plus syndrome  (9C40.8)
• Deafness - optic atrophy syndrome  (LD2H.Y)
• Autosomal dominant optic atrophy and cataract  (9C40.8)

synonyms

• Multiple mitochondrial DNA deletion syndromes
• Mitochondrial DNA deletion ataxia neuropathy spectrum
• Mitochondrial recessive ataxic syndrome
• MIRAS - [Mitochondrial recessive ataxic syndrome]
• Sensory ataxic neuropathy – dysarthria - ophthalmoparesis
• SANDO - [Sensory ataxic neuropathy – dysarthria - ophthalmoparesis] syndrome
• Spinocerebellar ataxia with epilepsy
• SCAE - [Spinocerebellar ataxia with epilepsy]

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