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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