Hypsarrhythmia

Symptom Information:

Symptom ID: HPO:0002521
Synonyms:
Hypsarrhythmia by EEG [HPO:0002521]
Hypsarrhythmia [OMIM:Hypsarrhythmia]
Hypsarrhythmia by EEG [OMIM:Hypsarrhythmia by EEG]
Hypsarrhythmia (in some patients) [OMIM:Hypsarrhythmia (in some patients)]
Quality:
Cross references:
OMIM: "Hypsarrhythmia" [OMIM:Hypsarrhythmia]
OMIM: "Hypsarrhythmia by EEG" [OMIM:Hypsarrhythmia by EEG]
OMIM: "Hypsarrhythmia (in some patients)" [OMIM:Hypsarrhythmia (in some patients)]
UMLS:C0684276 "Hypsarrhythmia" [HPO:0002521]
Is a (Direct Parents):
HPO         EEG with generalized epileptiform discharges
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:
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)