Epilepsy, familial temporal lobe, 3

Preferred Label : Epilepsy, familial temporal lobe, 3;

Symbol : ETL3;

CISMeF acronym : ETL3;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : FMTLE; Epilepsy, familial mesial temporal lobe;

Description : For a general description and a discussion of genetic heterogeneity of temporal lobe epilepsy, see ETL2 (608096).;

Inheritance : Autosomal dominant;

Prefixed ID : %611630;

Details

Origin ID

611630;

UMLS CUI

C1968848;

Currated CISMeF NLP mapping
- Benign familial mesial temporal lobe epilepsy [ORDO Disease]
- Benign familial mesial temporal lobe epilepsy (disorder) [SNOMED CT concept]
- epilepsy, familial mesial temporal lobe [MeSH concept]
- epilepsy, familial mesial temporal lobe [MeSH Supplementary Concept]
- familial temporal lobe epilepsy 3 [DO Concept]
DO Cross reference
- familial temporal lobe epilepsy 3 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Bilateral tonic-clonic seizure with focal onset [HPO term]
- Deja vu aura [HPO term]
- Epilepsy [HPO term]
- Focal impaired awareness seizure [HPO term]
Manual NTBT mappings (CISMeF)
- mesial temporal lobe epilepsy [Disease (Nov.)]
ORDO concept(s)
- Benign familial mesial temporal lobe epilepsy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Benign familial mesial temporal lobe epilepsy [ORDO Disease]
- epilepsy, familial mesial temporal lobe [MeSH Supplementary Concept]
- epilepsy, familial mesial temporal lobe [MeSH concept]
- familial temporal lobe epilepsy 3 [DO Concept]

Keyword's position in hierarchy(ies) :

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