febrile convulsions 2

Preferred Label : febrile convulsions 2;

Obsolete resource : true;

Approved symbol HGNC : FEB2;

Chromosome HGNC : 19p13.3;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:3644;

UMLS CUI

C1414577;

Automatic exact mappings (from CISMeF team)
- Epilepsy, idiopathic generalized, susceptibility to, 17 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients