Febrile seizures
Symptom Information:
Symptom ID: | HPO:0002373 | ||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |