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ICD-10-CM G40.83 — Dravet syndrome | Codelle

ICD-10-CM/G40.8/G40.83

G40.83

ICD-10-CM

Dravet syndrome

Clinical Notes

Inclusion Terms

Polymorphic epilepsy in infancy (PMEI)
Severe myoclonic epilepsy in infancy (SMEI)

Code Hierarchy

▲G40.8Other epilepsy and recurrent seizures

G40.83(current)

Subcodes (2)

G40.833Dravet syndrome, intractable, with status epilepticus

G40.834Dravet syndrome, intractable, without status epilepticus

Same Category

G40Epilepsy and recurrent seizures G40.0Local-rel (focal) idio epilepsy w seizures of loc onset G40.00Local-rel (focal) idio epi w seiz of loc onset, not ntrct G40.001Local-rel idio epi w seiz of loc onst, not ntrct, w stat epi G40.009Local-rel idio epi w seiz of loc onst,not ntrct,w/o stat epi G40.01Local-rel (focal) idio epi w seizures of loc onset, ntrct G40.011Local-rel idio epi w seiz of loc onset, ntrct, w stat epi G40.019Local-rel idio epi w seiz of loc onset, ntrct, w/o stat epi G40.1Local-rel (focal) symptc epilepsy w simple partial seizures G40.10Local-rel symptc epi w simple partial seiz, not ntrct

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