Hypsarrhythmia
Symptom Information:
Symptom ID: | HPO:0002521 | ||||
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) Abnormal nervous system electrophysiology(HPO:0001311) EEG abnormality(HPO:0002353) Epileptiform EEG discharges(HPO:0011182) EEG with generalized epileptiform discharges(HPO:0011198) Hypsarrhythmia(HPO:0002521) MedDRA: |
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Database Frequency: | 43 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
3-phosphoglycerate dehydrogenase deficiency | (Orphanet:79351) |
ALG2-CDG | (Orphanet:79326) |
ALG3-CDG | (Orphanet:79321) |
ASPARAGINE SYNTHETASE DEFICIENCY | (OMIM:615574) |
Amelo-cerebro-hypohidrotic syndrome | (Orphanet:1946) |
Atypical Rett syndrome | (Orphanet:3095) |
Beta-ureidopropionase deficiency | (Orphanet:65287) |
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5 | (OMIM:615763) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
D-glyceric aciduria | (Orphanet:941) |
DEND syndrome | (Orphanet:79134) |
DK1-CDG | (Orphanet:91131) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 | (OMIM:613722) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15 | (OMIM:615006) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17 | (OMIM:615473) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 | (OMIM:300672) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23 | (OMIM:615859) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26 | (OMIM:616056) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30 | (OMIM:616341) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4 | (OMIM:612164) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 | (OMIM:613477) |
Early infantile epileptic encephalopathy | (Orphanet:1934) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 5 | (OMIM:616025) |
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
Infantile epileptic-dyskinetic encephalopathy | (Orphanet:364063) |
Intellectual deficit, X-linked, Cantagrel type | (Orphanet:85277) |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY | (OMIM:613668) |
Malignant migrating partial seizures of infancy | (Orphanet:293181) |
Methylmalonic acidemia with homocystinuria, type cblX | (Orphanet:369962) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion | (Orphanet:363700) |
PEHO syndrome | (Orphanet:2836) |
PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE | (OMIM:608097) |
PERIVENTRICULAR NODULAR HETEROTOPIA 6 | (OMIM:615544) |
Permanent neonatal diabetes mellitus | (Orphanet:99885) |
Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome | (Orphanet:306558) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |
SLC35A2-CDG | (Orphanet:356961) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Spasticity - intellectual deficit - X-linked epilepsy | (Orphanet:3175) |
West syndrome | (Orphanet:3451) |
XYLOSIDASE DEFICIENCY | (OMIM:278900) |