Convulsive disorder, familial, with prenatal or early onset

Preferred Label : Convulsive disorder, familial, with prenatal or early onset;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 217200;

Détails

Origin ID

217200;

UMLS CUI

C1857575;

Currated CISMeF NLP mapping
- convulsive disorder, familial, with prenatal or early onset [MeSH concept]
- convulsive disorder, familial, with prenatal or early onset [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Death in infancy [HPO term]
- Intellectual disability [HPO term]
- Myoclonus [HPO term]
- Seizure [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- convulsive disorder, familial, with prenatal or early onset [MeSH Supplementary Concept]
- convulsive disorder, familial, with prenatal or early onset [MeSH concept]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients