Epileptic encephalopathy

Symptom Information:

Symptom ID: HPO:0200134
Synonyms:
Epileptic encephalopathy [OMIM:Epileptic encephalopathy]
Epileptic encephalopathy (in 2 of 3 patients) [OMIM:Epileptic encephalopathy (in 2 of 3 patients)]
Epileptic encephalopathy (in some patients) [OMIM:Epileptic encephalopathy (in some patients)]
Quality:
Cross references:
OMIM: "Epileptic encephalopathy" [OMIM:Epileptic encephalopathy]
OMIM: "Epileptic encephalopathy (in 2 of 3 patients)" [OMIM:Epileptic encephalopathy (in 2 of 3 patients)]
OMIM: "Epileptic encephalopathy (in some patients)" [OMIM:Epileptic encephalopathy (in some patients)]
Is a (Direct Parents):
HPO         Encephalopathy
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:
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)