Febrile seizures

Symptom Information:

Symptom ID: HPO:0002373
Synonyms:
Febrile convulsions [HPO:0002373]
Seizures, febrile, in early childhood [HPO:0002373]
Seizures, generalized, associated with fever [HPO:0002373]
Febrile seizures [OMIM:Febrile seizures]
Seizures, febrile, in early childhood [OMIM:Seizures, febrile, in early childhood]
Seizures, generalized, associated with fever [OMIM:Seizures, generalized, associated with fever]
Convulsions, febrile (in some patients) [OMIM:Convulsions, febrile (in some patients)]
Febrile seizures (1 patient) [OMIM:Febrile seizures (1 patient)]
Febrile seizures (in some) [OMIM:Febrile seizures (in some)]
Febrile seizures (reported in 1 patient) [OMIM:Febrile seizures (reported in 1 patient)]
Febrile seizures (usually remit by age 6 years) [OMIM:Febrile seizures (usually remit by age 6 years)]
Seizure, febrile (2/3 children) [OMIM:Seizure, febrile (2/3 children)]
Seizures, febrile (1 family) [OMIM:Seizures, febrile (1 family)]
Febrile convulsion [MedDRA:10016284]
Quality:
Cross references:
OMIM: "Febrile seizures" [OMIM:Febrile seizures]
OMIM: "Seizures, febrile, in early childhood" [OMIM:Seizures, febrile, in early childhood]
OMIM: "Seizures, generalized, associated with fever" [OMIM:Seizures, generalized, associated with fever]
OMIM: "Convulsions, febrile (in some patients)" [OMIM:Convulsions, febrile (in some patients)]
OMIM: "Febrile seizures (1 patient)" [OMIM:Febrile seizures (1 patient)]
OMIM: "Febrile seizures (in some)" [OMIM:Febrile seizures (in some)]
OMIM: "Febrile seizures (reported in 1 patient)" [OMIM:Febrile seizures (reported in 1 patient)]
OMIM: "Febrile seizures (usually remit by age 6 years)" [OMIM:Febrile seizures (usually remit by age 6 years)]
OMIM: "Seizure, febrile (2/3 children)" [OMIM:Seizure, febrile (2/3 children)]
OMIM: "Seizures, febrile (1 family)" [OMIM:Seizures, febrile (1 family)]
Is a (Direct Parents):
HPO         Seizures
MedDRA Seizures and seizure disorders NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Seizures(HPO:0001250)
                Febrile seizures(HPO:0002373)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Seizures(HPO:0001250)
       Seizures and seizure disorders NEC(MedDRA:10039912)
          Febrile seizures(HPO:0002373)
Database Frequency: 37 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 1 (Orphanet:67046)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
Bardet-Biedl syndrome 4 (OMIM:615982)
Benign familial neonatal seizures (Orphanet:1949)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Childhood absence epilepsy (Orphanet:64280)
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 (OMIM:607681)
EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 (OMIM:608096)
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10 (OMIM:613060)
EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 9 (OMIM:614280)
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET (OMIM:615369)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19 (OMIM:615744)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24 (OMIM:615871)
FEBRILE SEIZURES, FAMILIAL, 1 (OMIM:121210)
FEBRILE SEIZURES, FAMILIAL, 11 (OMIM:614418)
FEBRILE SEIZURES, FAMILIAL, 2 (OMIM:602477)
FEBRILE SEIZURES, FAMILIAL, 4 (OMIM:604352)
FEBRILE SEIZURES, FAMILIAL, 5 (OMIM:609255)
FEBRILE SEIZURES, FAMILIAL, 6 (OMIM:609253)
FEBRILE SEIZURES, FAMILIAL, 9 (OMIM:611634)
Familial infantile myoclonic epilepsy (Orphanet:352582)
Familial temporal epilepsy (Orphanet:98819)
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1 (OMIM:604233)
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2 (OMIM:604403)
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3 (OMIM:611277)
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 4 (OMIM:609800)
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7 (OMIM:613863)
Generalized epilepsy with febrile seizures-plus context (Orphanet:36387)
Hot water reflex epilepsy (Orphanet:166412)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
KEPPEN-LUBINSKY SYNDROME (OMIM:614098)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 7 (OMIM:614104)
MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIALBLOCK (OMIM:609438)
PACHYGYRIA, FRONTOTEMPORAL (OMIM:610279)
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE (OMIM:614066)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Wolfram syndrome 1 (OMIM:222300)