epilepsy, benign neonatal, autosomal recessive

Preferred Label : epilepsy, benign neonatal, autosomal recessive;

MeSH synonym : seizures, benign familial neonatal, autosomal recessive; convulsions, benign familial neonatal, autosomal recessive;

Details

Origin ID

C564823;

UMLS CUI

C1849250;

Automatic exact mappings (from CISMeF team)
- Seizures, benign familial neonatal, autosomal recessive [OMIM Phenotype]
MeSH term(s) associated for indexing
- epilepsy, benign neonatal [MeSH Descriptor]
Record concept(s)
- epilepsy, benign neonatal, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Seizures, benign familial neonatal, autosomal recessive [OMIM Phenotype]

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