Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
medical condition
epilepsy syndrome |
| gptkbp:alsoKnownAs |
Benign Familial Neonatal Epilepsy
|
| gptkbp:associatedWith |
gptkb:KCNQ2
gptkb:KCNQ3 |
| gptkbp:cause |
genetic disorder
|
| gptkbp:duration |
self-limited
|
| gptkbp:EEG_finding |
normal between seizures
|
| gptkbp:firstDescribed |
1964
|
| gptkbp:frequency |
rare
|
| https://www.w3.org/2000/01/rdf-schema#label |
Benign Neonatal Epilepsy
|
| gptkbp:ICD-10_code |
G40.3
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:OMIM |
121200
|
| gptkbp:onset |
neonatal period
|
| gptkbp:prognosis |
good
|
| gptkbp:seizureType |
focal seizures
generalized seizures |
| gptkbp:symptom |
seizures
|
| gptkbp:treatment |
anticonvulsant medication
|
| gptkbp:typicalAgeOfOnset |
first days of life
|
| gptkbp:bfsParent |
gptkb:D004239
|
| gptkbp:bfsLayer |
8
|