Febrile seizures, familial, 5

Preferred Label : Febrile seizures, familial, 5;

Symbol : FEB5;

CISMeF acronym : FEB5;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Convulsions, familial febrile, 5;

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

Inheritance : Autosomal dominant;

Prefixed ID : %609255;

Details

Origin ID

609255;

UMLS CUI

C1836507;

Automatic exact mappings (from CISMeF team)
- familial febrile seizures 5 [DO Concept]
- febrile convulsions 5 [HGNC gene]
- febrile convulsions, familial, 5 [MeSH Supplementary Concept]
- febrile convulsions, familial, 5 [MeSH concept]
DO Cross reference
- familial febrile seizures 5 [DO Concept]
HPO term(s)
- Atonic seizure [HPO term]
- Autosomal dominant inheritance [HPO term]
- Bilateral tonic-clonic seizure [HPO term]
- Childhood onset [HPO term]
- Children will develop afebrile seizure disorders later in life [HPO term]
- Epilepsy [HPO term]
- Febrile seizure (within the age range of 3 months to 6 years) [HPO term]
- Generalized tonic seizure [HPO term]
- Heterogeneous [HPO term]
- Hypertonic seizures [HPO term]
- Hypotonic seizures [HPO term]
- Onset 3 months of age up to 5 years [HPO term]
- Seizures occur in absence of intracranial infection or defined pathologic or traumatic cause [HPO term]
- Seizures usually last 1 to 5 minutes [HPO term]
- Seizures, generalized, associated with fever [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- febrile convulsions, familial, 5 [MeSH Supplementary Concept]
- febrile convulsions, familial, 5 [MeSH concept]

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