Seizures, benign familial neonatal, 3

Preferred Label : Seizures, benign familial neonatal, 3;

Symbol : BFNS3;

CISMeF acronym : BFNC3; BFNS3;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Convulsions, benign familial neonatal, 3; BFNC3;

Description : For a phenotypic description and a discussion of genetic heterogeneity of benign familial neonatal seizures, see BFNS1 (121200).;

Inheritance : Autosomal dominant;

Prefixed ID : %608217;

Détails

Origin ID

608217;

UMLS CUI

C1842382;

Automatic exact mappings (from CISMeF team)
- Benign familial neonatal epilepsy [ORDO Disease]
- epilepsy, benign neonatal, 3 [MeSH Supplementary Concept]
Broader ORDO disease(s)
- Benign familial neonatal epilepsy [ORDO Disease]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Bilateral tonic-clonic seizure [HPO term]
- Epilepsy [HPO term]
- Infantile onset [HPO term]
ORDO concept(s)
- Benign familial neonatal epilepsy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- epilepsy, benign neonatal, 3 [MeSH Supplementary Concept]
- epilepsy, benign neonatal, 3 [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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