Focal seizures

Symptom Information:

Symptom ID: HPO:0007359
Synonyms:
Partial seizures [HPO:0007359]
Seizures, partial, afebrile [HPO:0007359]
Focal seizures [OMIM:Focal seizures]
Partial seizures [OMIM:Partial seizures]
Seizures, partial, afebrile [OMIM:Seizures, partial, afebrile]
Seizures, focal [OMIM:Seizures, focal]
Seizures, partial [OMIM:Seizures, partial]
Partial seizures [MedDRA:10061334]
Quality:
Cross references:
OMIM: "Focal seizures" [OMIM:Focal seizures]
OMIM: "Partial seizures" [OMIM:Partial seizures]
OMIM: "Seizures, partial, afebrile" [OMIM:Seizures, partial, afebrile]
OMIM: "Seizures, focal" [OMIM:Seizures, focal]
OMIM: "Seizures, partial" [OMIM:Seizures, partial]
Is a (Direct Parents):
MedDRA Seizures and seizure disorders NEC
HPO         Seizures
HPO         Focal seizures, afebril
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)
                Focal seizures(HPO:0007359)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Seizures(HPO:0001250)
       Seizures and seizure disorders NEC(MedDRA:10039912)
          Focal seizures(HPO:0007359)
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant nocturnal frontal lobe epilepsy (Orphanet:98784)
Benign familial infantile seizures (Orphanet:306)
Benign familial neonatal-infantile seizures (Orphanet:140927)
CADASIL (Orphanet:136)
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3 (OMIM:613608)
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5 (OMIM:615400)
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10 (OMIM:613060)
EPILEPSY, NOCTURNAL FRONTAL LOBE, 5 (OMIM:615005)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 (OMIM:613722)
Early infantile epileptic encephalopathy without suppression burst (Orphanet:369894)
Epileptic encephalopathy with continuous spike-and-wave during sleep (Orphanet:725)
Familial infantile myoclonic epilepsy (Orphanet:352582)
Female restricted epilepsy with intellectual deficit (Orphanet:101039)
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 7 (OMIM:613863)
Infantile convulsions and choreoathetosis (Orphanet:31709)
Landau-Kleffner syndrome (Orphanet:98818)
Leigh syndrome (Orphanet:506)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 (OMIM:614563)
Malignant migrating partial seizures of infancy (Orphanet:293181)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
ROLANDIC EPILEPSY, MENTAL RETARDATION, AND SPEECH DYSPRAXIA, X-LINKED (OMIM:300643)
SEIZURES, BENIGN FAMILIAL INFANTILE, 1 (OMIM:601764)
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 (OMIM:605751)
Sneddon syndrome (Orphanet:820)
X-linked epilepsy - learning disabilities - behavior disorders (Orphanet:85294)