G40.83
Dravet syndrome
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This code does not map to a risk-adjusting HCC in the loaded models.
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
Polymorphic epilepsy in infancy (PMEI) Severe myoclonic epilepsy in infancy (SMEI)
Epilepsies and epileptic syndromes undetermined as to whether they are focal or generalized Landau-Kleffner syndrome
conversion disorder with seizures (F44.5) convulsions NOS (R56.9) post traumatic seizures (R56.1) seizure (convulsive) NOS (R56.9) seizure of newborn (P90)
hippocampal sclerosis (G93.81) mesial temporal sclerosis (G93.81) temporal sclerosis (G93.81) Todd's paralysis (G83.84)
the following terms are to be considered equivalent to intractable: pharmacoresistant (pharmacologically resistant), treatment resistant, refractory (medically) and poorly controlled
certain conditions originating in the perinatal period (P04-P96) certain infectious and parasitic diseases (A00-B99) complications of pregnancy, childbirth and the puerperium (O00-O9A) congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99) endocrine, nutritional and metabolic diseases (E00-E88) injury, poisoning and certain other consequences of external causes (S00-T88) neoplasms (C00-D49) symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)