Dravet syndrome
ICD-10 Code
G40.83
Dravet syndrome
Definition
Dravet syndrome is a channelopathy with epilepsy of with onset during the first year of life, typically 4-5 months, characterized by status epilepticus and a variety of drug-resistant seizures often induced by fever, presenting in previously healthy children, and which frequently leads to cognitive and motor impairment. Dravet differs from other channelopathies usually due to a mutation in SCN1A.
Also known as Dravet, Dravet syndrome, DS, myoclonic epilepsy, severe, of infancy, severe myoclonic epilepsy of infancy, SME, SMEB — per MONDO
Also identified as
- DOID 0060171 per MONDO
- DOID 0080422 per MONDO
- ICD10CM G40.83 per MONDO
- ICD9 345.10 per MONDO
- NCIT C116573 per MONDO
- SCTID 230437002 per MONDO
- UMLS C0751122 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Brain | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Brain | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Central nervous system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Central nervous system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Nervous system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Nervous system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |