Epileptic spasms
Symptom Information:
Symptom ID: | HPO:0011097 | ||||||||
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) Epileptic spasms(HPO:0011097) MedDRA: |
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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) |