epilepsy, benign neonatal

Preferred Label : epilepsy, benign neonatal;

MeSH definition : A condition marked by recurrent seizures that occur during the first 4-6 weeks of life despite an otherwise benign neonatal course. Autosomal dominant familial and sporadic forms have been identified. Seizures generally consist of brief episodes of tonic posturing and other movements, apnea, eye deviations, and blood pressure fluctuations. These tend to remit after the 6th week of life. The risk of developing epilepsy at an older age is moderately increased in the familial form of this disorder. (Neurologia 1996 Feb;11(2):51-5);

MeSH synonym : benign neonatal convulsions; convulsions, benign neonatal; benign neonatal epilepsies; benign neonatal epilepsy; epilepsies, benign neonatal; neonatal epilepsies, benign; neonatal epilepsy, benign; neonatal convulsions, benign; benign neonatal convulsion; convulsion, benign neonatal; neonatal convulsion, benign;

MeSH hyponym : benign neonatal epilepsy, nonfamilial; convulsions, benign familial infantile, 3; benign familial neonatal epilepsy; Benign Familial Infantile Convulsions Syndrome; Benign Familial Neonatal Convulsions; Benign Familial Neonatal-Infantile Seizures; Benign Familial Neonatal Infantile Seizures; Benign Infantile Familial Convulsions; Convulsions Benign Familial Neonatal; Convulsions, Benign Familial Infantile, 1; Convulsions, Benign Neonatal, Familial; Epilepsy, Benign Neonatal, Familial; Epilepsy, Benign Neonatal-Infantile; Benign Neonatal-Infantile Epilepsies; Benign Neonatal-Infantile Epilepsy; Epilepsies, Benign Neonatal-Infantile; Epilepsy, Benign Neonatal Infantile; Neonatal-Infantile Epilepsies, Benign; Neonatal-Infantile Epilepsy, Benign; Familial Benign Neonatal Convulsions; Familial Benign Neonatal Epilepsy; Seizures, Benign Familial Infantile, 1; Seizures, Benign Familial Neonatal-Infantile; Seizures, Benign Familial Neonatal Infantile; Benign Familial Infantile Convulsions; Benign Neonatal Non-Familial Convulsions; Benign Neonatal Non Familial Convulsions; Benign Neonatal Nonfamilial Epilepsy; Non-Familial Benign Neonatal Convulsions; Non Familial Benign Neonatal Convulsions; Convulsions, Benign Neonatal, Non-Familial; Epilepsy, Benign Neonatal, Non-Familial; Epilepsy, Benign Neonatal, Nonfamilial; Non-Familial Benign Neonatal Epilepsy; Non Familial Benign Neonatal Epilepsy; Benign Non-Familial Neonatal Convulsions; Benign Non Familial Neonatal Convulsions; Seizures, Benign Familial Infantile, 3;

Details

Origin ID

D020936;

UMLS CUI

C0270851;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Benign Familial Infantile Seizures [NCIt concept]
- Benign idiopathic neonatal seizures [ORDO Disease]
- Benign neonatal convulsions (disorder) [SNOMED CT concept]
- Generalized idiopathic epilepsy and epileptic syndromes [ICD-10 Sub-category (who)]
- Seizures, benign familial infantile, 1 [OMIM Phenotype]
- benign neonatal convulsions [SNOMED Notion]
- benign neonatal seizures [DO Concept]
Currated CISMeF NLP mapping
- Benign Neonatal Epilepsy [NCIt concept]
- Benign familial infantile epilepsy [ORDO Disease]
- Benign familial neonatal convulsions [MedDRA Preferred Term]
- Benign familial neonatal epilepsy [ICD-11 More detail]
- 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.)]
DO Cross reference
- benign familial neonatal epilepsy [DO Concept]
- benign neonatal seizures [DO Concept]
Manual BTNT mappings - CISMeF
- Familial or sporadic hemiplegic migraine [ORDO Disease]
- Infantile convulsions and choreoathetosis [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Benign partial infantile seizures [ORDO Disease]
- Channelopathy due to a voltage-gated potassium channel defect [ORDO Disease]
- Channelopathy due to a voltage-gated sodium channel defect [ORDO Disease]
- Channelopathy with epilepsy [ORDO Disease]
- Familial partial epilepsy [ORDO Disease]
- Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes [ORDO Disease]
- Infantile epilepsy syndrome [ORDO Disease]
- Neonatal epilepsy syndrome [ORDO Disease]
- Neurological channelopathy of the central nervous system due to a genetic potassium channel defect [ORDO Disease]
ORDO relation(s)
- Benign familial neonatal epilepsy [ORDO Disease]
Record concept(s)
- Benign Familial Neonatal Epilepsy [MeSH concept]
- Benign Infantile Familial Convulsions [MeSH concept]
- Epilepsy, Benign Neonatal-Infantile [MeSH concept]
- Seizures, Benign Familial Infantile, 1 [MeSH concept]
- benign neonatal epilepsy, nonfamilial [MeSH concept]
- convulsions, benign familial infantile, 3 [MeSH concept]
- epilepsy, benign neonatal [MeSH concept]
Related MeSH Supplementary Concept(s)
- Convulsions, Benign Familial Neonatal, 1, And-Or Myokymia [MeSH Supplementary Concept]
- convulsions benign familial neonatal dominant form [MeSH Supplementary Concept]
- convulsions, benign familial infantile, 4 [MeSH Supplementary Concept]
- convulsions, benign familial neonatal, 1, atypical severe [MeSH Supplementary Concept]
- epilepsy, benign neonatal, 1 [MeSH Supplementary Concept]
- epilepsy, benign neonatal, 1, atypical severe [MeSH Supplementary Concept]
- epilepsy, benign neonatal, 3 [MeSH Supplementary Concept]
- epilepsy, benign neonatal, autosomal recessive [MeSH Supplementary Concept]
- infantile convulsions and paroxysmal choreoathetosis, familial [MeSH Supplementary Concept]
- myokymia with neonatal epilepsy [MeSH Supplementary Concept]
See also inter- (CISMeF)
- Benign familial neonatal-infantile seizures (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Benign Neonatal Epilepsy [NCIt concept]
- Benign neonatal convulsions (disorder) [SNOMED CT concept]
- benign neonatal convulsions [SNOMED Notion]
- benign neonatal seizures [DO Concept]
Validated automatic mappings to BTNT
- Benign familial neonatal epilepsy [ORDO Disease]
- Benign non-familial neonatal convulsions (disorder) [SNOMED CT concept]
- Seizures, benign familial infantile, 3 [OMIM Phenotype]
- benign familial neonatal epilepsy [DO Concept]

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