Benign Neonatal Epilepsy

Preferred Label : Benign Neonatal Epilepsy;

NCIt definition : An inherited or sporadic disorder characterized by epileptic seizures in the first four to six weeks of life. The seizures tend to subside after the fifteenth week of life.;

Details

Origin ID

C84593;

UMLS CUI

C0270851;

Currated CISMeF NLP mapping
- Benign familial infantile epilepsy [ORDO Disease]
- Benign familial neonatal convulsions [MedDRA Preferred Term]
- Benign familial neonatal-infantile seizures [ORDO Disease]
- Benign neonatal familial convulsions (disorder) [SNOMED CT concept]
- Familial neonatal seizures (disorder) [SNOMED CT concept]
- benign familial infantile epilepsy [DO Concept]
- benign familial neonatal convulsion [Disease (Nov.)]
- epilepsy, benign neonatal [MeSH Descriptor]
- epilepsy, benign neonatal [MeSH concept]
DO Cross reference
- benign neonatal seizures [DO Concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Benign neonatal convulsions (disorder) [SNOMED CT concept]
- benign neonatal convulsions [SNOMED Notion]
- benign neonatal seizures [DO Concept]
- epilepsy, benign neonatal [MeSH concept]
- epilepsy, benign neonatal [MeSH Descriptor]
Validated automatic mappings to BTNT
- Benign familial neonatal epilepsy [ORDO Disease]
disease_has_primary_anatomic_site
- Brain [NCIt concept]

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