Absence seizures
Symptom Information:
Symptom ID: | HPO:0002121 | ||||||||||||||||||||||
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) Generalized seizures(HPO:0002197) Absence seizures(HPO:0002121) Dialeptic seizures(HPO:0011146) Absence seizures(HPO:0002121) MedDRA: Nervous system disorders(MedDRA:10029205) Seizures(HPO:0001250) Absence seizures(HPO:0002121) |
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Database Frequency: | 62 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 1 | (Orphanet:67046) |
3-methylglutaconic aciduria type 4 | (Orphanet:67048) |
4-hydroxybutyric aciduria | (Orphanet:22) |
48,XXYY syndrome | (Orphanet:10) |
Alström syndrome | (Orphanet:64) |
Argininemia | (Orphanet:90) |
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
Bangstad syndrome | (Orphanet:1227) |
CADASIL | (Orphanet:136) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Childhood absence epilepsy | (Orphanet:64280) |
Classical phenylketonuria | (Orphanet:79254) |
Constitutional megaloblastic anemia with severe neurologic disease | (Orphanet:319651) |
Dravet syndrome | (Orphanet:33069) |
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 1 | (OMIM:600131) |
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 | (OMIM:607681) |
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5 | (OMIM:612269) |
EPILEPSY, IDIOPATHIC GENERALIZED | (OMIM:600669) |
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10 | (OMIM:613060) |
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11 | (OMIM:607628) |
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12 | (OMIM:614847) |
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9 | (OMIM:607682) |
EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 9 | (OMIM:614280) |
EPILEPSY, MYOCLONIC JUVENILE | (OMIM:254770) |
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET | (OMIM:615369) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19 | (OMIM:615744) |
Early infantile epileptic encephalopathy without suppression burst | (Orphanet:369894) |
FEBRILE SEIZURES, FAMILIAL, 9 | (OMIM:611634) |
Female restricted epilepsy with intellectual deficit | (Orphanet:101039) |
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 7 | (OMIM:613863) |
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9 | (OMIM:616172) |
Generalized epilepsy - paroxysmal dyskinesia | (Orphanet:79137) |
Generalized epilepsy with febrile seizures-plus context | (Orphanet:36387) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
HERNS syndrome | (Orphanet:63261) |
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency | (Orphanet:83639) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Juvenile absence epilepsy | (Orphanet:1941) |
Juvenile myoclonic epilepsy | (Orphanet:307) |
Lafora disease | (Orphanet:501) |
Leigh syndrome | (Orphanet:506) |
Lymphangioleiomyomatosis | (Orphanet:538) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG | (OMIM:254800) |
Maple syrup urine disease | (Orphanet:511) |
Menkes disease | (Orphanet:565) |
Microduplication Xp11.22-p11.23 syndrome | (Orphanet:217377) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Niemann-Pick disease type C | (Orphanet:646) |
Occipital pachygyria and polymicrogyria | (Orphanet:280640) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Progressive myoclonic epilepsy type 6 | (Orphanet:280620) |
Tyrosinemia type 2 | (Orphanet:28378) |
Unverricht-Lundborg disease | (Orphanet:308) |
Wilson-Turner syndrome | (Orphanet:3459) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
Wolfram syndrome | (Orphanet:3463) |