Epileptic spasms

Symptom Information:

Symptom ID: HPO:0011097
Synonyms:
Salaam convulsions [HPO:0011097]
Salaam seizures [HPO:0011097]
West syndrome [HPO:0011097]
Epileptic spasm [Orphanet:43390]
Epileptic spasms [OMIM:Epileptic spasms]
West syndrome [OMIM:West syndrome]
Seizures/epilepsy/absences/spasms/status epilepticus [Orphanet:43390]
Epilepsy [IBIS, cm]
Quality:
Cross references:
Orphanet:43390 "Seizures/epilepsy/absences/spasms/status epilepticus" [Orphanet:43390]
OMIM: "Epileptic spasms" [OMIM:Epileptic spasms]
OMIM: "West syndrome" [OMIM:West syndrome]
Is a (Direct Parents):
HPO         Seizures
Orphanet Seizures
Orphanet Functional anomalies of the nervous system
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)
                Epileptic spasms(HPO:0011097)
MedDRA:
Database Frequency: 45 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
3-methylglutaconic aciduria type 1 (Orphanet:67046)
3-methylglutaconic aciduria type 4 (Orphanet:67048)
48,XXYY syndrome (Orphanet:10)
Adenylosuccinate lyase deficiency (Orphanet:46)
Aicardi syndrome (Orphanet:50)
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)
DK1-CDG (Orphanet:91131)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13 (OMIM:614558)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15 (OMIM:615006)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4 (OMIM:612164)
Familial long QT syndrome (Orphanet:768)
Gaucher disease type 2 (Orphanet:77260)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
HERNS syndrome (Orphanet:63261)
Hyperlysinemia, type I (OMIM:238700)
Jervell and Lange-Nielsen syndrome (Orphanet:90647)
Leigh syndrome (Orphanet:506)
Long QT syndrome 1 (OMIM:192500)
Long QT syndrome 2 (OMIM:613688)
Long QT syndrome 3 (OMIM:603830)
Lymphangioleiomyomatosis (Orphanet:538)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
Maple syrup urine disease (Orphanet:511)
Menkes disease (Orphanet:565)
Mowat-Wilson syndrome (Orphanet:2152)
Niemann-Pick disease type C (Orphanet:646)
Partial acquired lipodystrophy (Orphanet:79087)
Romano-Ward syndrome (Orphanet:101016)
Short chain acyl-CoA dehydrogenase deficiency (Orphanet:26792)
Sino-auricular heart block (Orphanet:1260)
Sneddon syndrome (Orphanet:820)
Tyrosinemia type 2 (Orphanet:28378)
West syndrome (Orphanet:3451)
Wilson-Turner syndrome (Orphanet:3459)
Wolcott-Rallison syndrome (Orphanet:1667)
Wolfram syndrome (Orphanet:3463)