Febrile seizures, familial, 7

Preferred Label : Febrile seizures, familial, 7;

Symbol : FEB7;

CISMeF acronym : FEB7;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : FEB7; Febrile convulsions, familial, 7;

Description : For a phenotypic description of familial febrile seizures and a discussion of genetic heterogeneity of this disorder, see FEB1 (121210).;

Prefixed ID : %611515;

Details

Origin ID

611515;

UMLS CUI

C1969087;

Automatic exact mappings (from CISMeF team)
- familial febrile seizures 7 [DO Concept]
- febrile convulsions 7 [HGNC gene]
- febrile convulsions, familial, 7 [MeSH Supplementary Concept]
- febrile convulsions, familial, 7 [MeSH concept]
DO Cross reference
- familial febrile seizures 7 [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- febrile convulsions, familial, 7 [MeSH Supplementary Concept]
- febrile convulsions, familial, 7 [MeSH concept]

Keyword's position in hierarchy(ies) :

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