convulsions, benign familial infantile, 2 - CISMeF

" /> convulsions, benign familial infantile, 2 - CISMeF

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Convulsions, benign familial infantile, 2MeSH Supplementary Concept

Preferred Label : convulsions, benign familial infantile, 2;

MeSH note : mutation in PRRT2;

MeSH synonym : seizures, benign familial infantile, 2;

Details

Origin ID

C565296;

UMLS CUI

C1853995;

Automatic exact mappings (from CISMeF team)
- Seizures, benign familial infantile, 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- spasms, infantile [MeSH Descriptor]
Record concept(s)
- convulsions, benign familial infantile, 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Seizures, benign familial infantile, 2 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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02/05/2025

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