8A61.0Y Other specified genetic epileptic syndromes with neonatal onset
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
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
- Other specified genetic epileptic syndromes with neonatal onset
- Benign familial neonatal epilepsy
- Benign familial neonatal seizures
- Early myoclonic encephalopathy
- Pyridoxine dependent epilepsy with antiquitin mutations
- Glutamate decarboxylase deficiency
- Pyridoxine-responsive seizures
- Vitamin B6-responsive seizures
- Pyridoxine-dependent seizures
- Epilepsy due to vitamin B6 or pyridoxine deficiency
- Cerebral folate deficiency
- Other genetic epileptic syndromes with neonatal onset
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