Typical absence seizures

Symptom Information:

Symptom ID: HPO:0011147
Synonyms:
Petit mal seizures [HPO:0011147]
Absence seizure [Orphanet:43390]
Absence seizure (disorder) [Orphanet:43390]
Childhood absence epilepsy (disorder) [Orphanet:43390]
Absence Epilepsy [Orphanet:43390]
Seizures/epilepsy/absences/spasms/status epilepticus [Orphanet:43390]
Petit mal epilepsy [Orphanet:43390]
Petit mal epilepsy [MedDRA:10034759]
Abscences [MedDRA:10034759]
Absence attacks [MedDRA:10034759]
Absence seizure [MedDRA:10034759]
Convulsion petit mal [MedDRA:10034759]
Epilepsy petit mal [MedDRA:10034759]
Petit mal [MedDRA:10034759]
Petit mal convulsion [MedDRA:10034759]
Petit mal status, epileptic [MedDRA:10034759]
Status epilepticus petit mal [MedDRA:10034759]
Atypical petit mal [MedDRA:10034759]
Absence seizures (in some) [OMIM:Absence seizures (in some)]
Absence seizures (stage 2 and 3) [OMIM:Absence seizures (stage 2 and 3)]
Seizures, absence [OMIM:Seizures, absence]
Absence seizures [MedDRA:10000332]
Quality:
Cross references:
HPO:0002121 "Absence seizures" [Orphanet:43390]
Orphanet:43390 "Seizures/epilepsy/absences/spasms/status epilepticus" [Orphanet:43390]
OMIM: "Absence seizures (in some)" [OMIM:Absence seizures (in some)]
OMIM: "Absence seizures (stage 2 and 3)" [OMIM:Absence seizures (stage 2 and 3)]
OMIM: "Seizures, absence" [OMIM:Seizures, absence]
UMLS:C0014553 "Absence Epilepsy" [Orphanet:43390]
Is a (Direct Parents):
MedDRA Seizures
Orphanet Functional anomalies of the nervous system
Orphanet Seizures
MedDRA Absence seizures
HPO         Absence seizures
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)
                      Typical absence seizures(HPO:0011147)
                Dialeptic seizures(HPO:0011146)
                   Absence seizures(HPO:0002121)
                      Typical absence seizures(HPO:0011147)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Seizures(HPO:0001250)
       Absence seizures(HPO:0002121)
          Typical absence seizures(HPO:0011147)
       Typical absence seizures(HPO:0011147)
Database Frequency: 33 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 1 (Orphanet:67046)
3-methylglutaconic aciduria type 4 (Orphanet:67048)
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)
Classical phenylketonuria (Orphanet:79254)
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12 (OMIM:614847)
EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 9 (OMIM:614280)
Female restricted epilepsy with intellectual deficit (Orphanet:101039)
Generalized epilepsy - paroxysmal dyskinesia (Orphanet:79137)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
HERNS syndrome (Orphanet:63261)
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (Orphanet:83639)
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)
Mowat-Wilson syndrome (Orphanet:2152)
Niemann-Pick disease type C (Orphanet:646)
Occipital pachygyria and polymicrogyria (Orphanet:280640)
Partial acquired lipodystrophy (Orphanet:79087)
Tyrosinemia type 2 (Orphanet:28378)
Wilson-Turner syndrome (Orphanet:3459)
Wolcott-Rallison syndrome (Orphanet:1667)
Wolfram syndrome (Orphanet:3463)