Epileptic encephalopathy
Symptom Information:
Symptom ID: | HPO:0200134 | |||
Synonyms: |
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Quality: | ||||
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 morphology(HPO:0012639) Morphological abnormality of the central nervous system(HPO:0002011) Encephalopathy(HPO:0001298) Epileptic encephalopathy(HPO:0200134) MedDRA: |
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Database Frequency: | 42 / 7739 | |||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
5q14.3 microdeletion syndrome | (Orphanet:228384) |
Amelo-cerebro-hypohidrotic syndrome | (Orphanet:1946) |
Atypical Rett syndrome | (Orphanet:3095) |
Beta-mannosidosis | (Orphanet:118) |
COENZYME Q10 DEFICIENCY, PRIMARY, 7 | (OMIM:616276) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Dravet syndrome | (Orphanet:33069) |
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET | (OMIM:615369) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 | (OMIM:613721) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13 | (OMIM:614558) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14 | (OMIM:614959) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15 | (OMIM:615006) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17 | (OMIM:615473) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19 | (OMIM:615744) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21 | (OMIM:615833) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23 | (OMIM:615859) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24 | (OMIM:615871) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25 | (OMIM:615905) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26 | (OMIM:616056) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27 | (OMIM:616139) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 | (OMIM:616211) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4 | (OMIM:612164) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 | (OMIM:613477) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 | (OMIM:613720) |
Early infantile epileptic encephalopathy | (Orphanet:1934) |
Early infantile epileptic encephalopathy without suppression burst | (Orphanet:369894) |
Early myoclonic encephalopathy | (Orphanet:1935) |
Hyperekplexia - epilepsy | (Orphanet:163985) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY | (OMIM:606369) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 5 | (OMIM:612621) |
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 | (OMIM:614299) |
Malignant migrating partial seizures of infancy | (Orphanet:293181) |
Microcephaly - seizures - developmental delay | (Orphanet:228418) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome | (Orphanet:457185) |
Pitt-Hopkins-like syndrome 2 | (OMIM:614325) |
Progressive myoclonic epilepsy with dystonia | (Orphanet:352596) |
SLC35A2-CDG | (Orphanet:356961) |
West syndrome | (Orphanet:3451) |