Focal seizures
Symptom Information:
Symptom ID: | HPO:0007359 | ||||||||
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) Focal seizures(HPO:0007359) MedDRA: Nervous system disorders(MedDRA:10029205) Seizures(HPO:0001250) Seizures and seizure disorders NEC(MedDRA:10039912) Focal seizures(HPO:0007359) |
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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) |