epilepsy, nocturnal frontal lobe, type 4

Preferred Label : epilepsy, nocturnal frontal lobe, type 4;

MeSH note : mutation in CHRNA2;

MeSH synonym : epilepsy, familial, with nocturnal wandering and ictal fear;

Details

Origin ID

C563679;

UMLS CUI

C1835905;

Currated CISMeF NLP mapping
- Epilepsy, nocturnal frontal lobe, 4 [OMIM Phenotype]
- autosomal dominant nocturnal frontal lobe epilepsy 4 [DO Concept]
MeSH term(s) associated for indexing
- epilepsy, frontal lobe [MeSH Descriptor]
- somnambulism [MeSH Descriptor]
Record concept(s)
- epilepsy, nocturnal frontal lobe, type 4 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Epilepsy, nocturnal frontal lobe, 4 [OMIM Phenotype]
- autosomal dominant nocturnal frontal lobe epilepsy 4 [DO Concept]

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