8A60.A Epilepsy due to genetic syndromes with widespread or progressive effects
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Epilepsy due to genetically determined conditions in which, as we currently understand it, there is a separate disorder interposed between the genetic defect and the epilepsy, for example, as in tuberous sclerosis. Includes epilepsy due to documented autosomal, X-linked, mitochondrial or chromosomal abnormalities.
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed
synonyms
- Epilepsy due to genetic syndromes with widespread or progressive effects
- Epilepsy due to autosomal recessive genetic syndromes with widespread or progressive effects
- Epilepsy due to autosomal dominant genetic syndromes with widespread or progressive effects
- Epilepsy due to X-linked recessive progressive myoclonic epilepsy with ataxia
- Epilepsy due to mitochondrial disorders
- Mitochondrial encephalomyopathies
- Epilepsy due to chromosomal disorders
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