Epilepsy, benign occipital

Preferred Label : Epilepsy, benign occipital;

Symbol : BOE;

CISMeF acronym : BOE;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 132090;

Details

Origin ID

132090;

UMLS CUI

C1851549;

Automatic exact mappings (from CISMeF team)
- Benign occipital epilepsy [ICD-11 More detail]
- Benign occipital lobe epilepsy (disorder) [SNOMED CT concept]
- epilepsies, partial [MeSH Descriptor]
Currated CISMeF NLP mapping
- Benign occipital epilepsy [ORDO Disease]
- benign occipital epilepsy [MeSH concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- EEG abnormality [HPO term]
- Epilepsy [HPO term]
- Seizure [HPO term]
ORDO concept(s)
- Benign occipital epilepsy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Benign occipital epilepsy [ORDO Disease]
- Benign occipital lobe epilepsy (disorder) [SNOMED CT concept]
- benign occipital epilepsy [MeSH concept]

Keyword's position in hierarchy(ies) :

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