EEG abnormality
Symptom Information:
Symptom ID: | HPO:0002353 | |||||||||||||
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 physiology(HPO:0012638) Abnormal nervous system electrophysiology(HPO:0001311) EEG abnormality(HPO:0002353) MedDRA: Investigations(MedDRA:10022891) Neurological, special senses and psychiatric investigations(MedDRA:10029295) Neurologic diagnostic procedures(MedDRA:10029285) EEG abnormality(HPO:0002353) |
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Database Frequency: | 188 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
15q11q13 microduplication syndrome | (Orphanet:238446) |
16p13.11 microdeletion syndrome | (Orphanet:261236) |
17p11.2 microduplication syndrome | (Orphanet:1713) |
1p36 deletion syndrome | (Orphanet:1606) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
4-hydroxybutyric aciduria | (Orphanet:22) |
6q16 deletion syndrome | (Orphanet:171829) |
AUTISM | (OMIM:209850) |
AUTISM, SUSCEPTIBILITY TO, 3 | (OMIM:608049) |
AUTISM, SUSCEPTIBILITY TO, 8 | (OMIM:607373) |
AUTISM, SUSCEPTIBILITY TO, X-LINKED 1 | (OMIM:300425) |
AUTISM, SUSCEPTIBILITY TO, X-LINKED 2 | (OMIM:300495) |
AUTISM, SUSCEPTIBILITY TO, X-LINKED 3 | (OMIM:300496) |
Acro-oto-ocular syndrome | (Orphanet:2980) |
Adams-Oliver syndrome | (Orphanet:974) |
Aicardi syndrome | (Orphanet:50) |
Alexander disease | (Orphanet:58) |
Alopecia - epilepsy - pyorrhea - intellectual deficit | (Orphanet:1008) |
Alopecia-intellectual deficit syndrome | (Orphanet:2850) |
Alpers syndrome | (Orphanet:726) |
Amelo-cerebro-hypohidrotic syndrome | (Orphanet:1946) |
Angelman syndrome | (Orphanet:72) |
Argininemia | (Orphanet:90) |
Argininosuccinic aciduria | (Orphanet:23) |
Arthrogryposis multiplex congenita - whistling face | (Orphanet:1150) |
Atypical Rett syndrome | (Orphanet:3095) |
Autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency | (Orphanet:308410) |
Bangstad syndrome | (Orphanet:1227) |
Benign adult familial myoclonic epilepsy | (Orphanet:86814) |
Benign occipital epilepsy | (Orphanet:25968) |
Bilateral generalized polymicrogyria | (Orphanet:208447) |
Bird headed-dwarfism, Montreal type | (Orphanet:2617) |
Bonnemann-Meinecke-Reich syndrome | (Orphanet:1261) |
Borjeson-Forssman-Lehmann syndrome | (Orphanet:127) |
CADASIL | (Orphanet:136) |
CEREBROOCULOFACIOSKELETAL SYNDROME 4 | (OMIM:610758) |
CLN1 disease | (Orphanet:228329) |
CLN11 disease | (Orphanet:314629) |
CLN7 disease | (Orphanet:228366) |
CLN8 disease | (Orphanet:228354) |
Canavan disease | (Orphanet:141) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Carnosinemia | (Orphanet:1361) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Central bilateral macrogyria | (Orphanet:2431) |
Cerebral gigantism - jaw cysts | (Orphanet:2081) |
Cerebrotendinous xanthomatosis | (Orphanet:909) |
Cockayne syndrome | (Orphanet:191) |
Cogan syndrome | (Orphanet:1467) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
Corneal-cerebellar syndrome | (Orphanet:3177) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
DPM1-CDG | (Orphanet:79322) |
Deafness - onychodystrophy | (Orphanet:3231) |
Deafness - vitiligo - achalasia | (Orphanet:3239) |
Dehydratase deficiency | (Orphanet:1578) |
Dihydropteridine reductase deficiency | (Orphanet:226) |
Dwarfism - intellectual deficit - eye abnormality | (Orphanet:2650) |
ELECTROENCEPHALOGRAM, LOW-VOLTAGE | (OMIM:130180) |
ELECTROENCEPHALOGRAPHIC PATTERN, BETA FREQUENCY, QUANTITATIVE TRAITLOCUS | (OMIM:130190) |
ELECTROENCEPHALOGRAPHIC PECULIARITY: 14 AND 6 PER SEC. POSITIVE SPIKEPHENOMENON | (OMIM:130200) |
ELECTROENCEPHALOGRAPHIC PECULIARITY: FRONTO-PRECENTRAL BETA WAVE GROUPS | (OMIM:130300) |
ELECTROENCEPHALOGRAPHIC PECULIARITY: OCCIPITAL SLOW BETA WAVES | (OMIM:130400) |
EPILEPSY, PROGRESSIVE MYOCLONIC, 5 | (OMIM:613832) |
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET | (OMIM:615369) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 | (OMIM:300672) |
Early infantile epileptic encephalopathy without suppression burst | (Orphanet:369894) |
Encephalopathy due to GLUT1 deficiency | (Orphanet:71277) |
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria | (Orphanet:1035) |
Facial asymmetry - temporal seizures | (Orphanet:1167) |
Familial or sporadic hemiplegic migraine | (Orphanet:569) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Febrile infection-related epilepsy syndrome | (Orphanet:163703) |
Flynn-Aird syndrome | (Orphanet:2047) |
Fountain syndrome | (Orphanet:3219) |
Galloway-Mowat syndrome | (Orphanet:2065) |
Gingival fibromatosis-hypertrichosis syndrome | (Orphanet:2026) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Hartnup syndrome | (Orphanet:2116) |
Hereditary myoclonus - progressive distal muscular atrophy | (Orphanet:2590) |
Hernandez-Aguirre Negrete syndrome | (Orphanet:2139) |
Huntington disease | (Orphanet:399) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Hyperlysinemia, type I | (OMIM:238700) |
Hyperprolinemia type 1 | (Orphanet:419) |
Hypertryptophanemia | (Orphanet:2224) |
Infantile convulsions and choreoathetosis | (Orphanet:31709) |
Infantile neuronal ceroid lipofuscinosis | (Orphanet:79263) |
Infantile spasms - broad thumbs | (Orphanet:3173) |
Intellectual deficit, X-linked - hypotonia - facial dysmorphism - aggressive behavior | (Orphanet:85329) |
Intellectual deficit, X-linked - psychosis - macroorchidism | (Orphanet:3077) |
Intellectual deficit, X-linked, Brooks type | (Orphanet:3056) |
Intellectual deficit, X-linked, Vitale type | (Orphanet:85289) |
Intellectual deficit, X-linked, Wittwer type | (Orphanet:85291) |
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome | (Orphanet:369837) |
Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
Isolated glycerol kinase deficiency | (Orphanet:408) |
Juvenile neuronal ceroid lipofuscinosis | (Orphanet:79264) |
KBG syndrome | (Orphanet:2332) |
KRABBE DISEASE | (OMIM:245200) |
Kabuki syndrome | (Orphanet:2322) |
Kenny-Caffey syndrome | (Orphanet:2333) |
Krabbe disease | (Orphanet:487) |
Late infantile neuronal ceroid lipofuscinosis | (Orphanet:168491) |
Leigh syndrome with nephrotic syndrome | (Orphanet:255249) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
MEHMO syndrome | (Orphanet:85282) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY,AND SHORT STATURE | (OMIM:609037) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 5 | (OMIM:612621) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 6 | (OMIM:613970) |
MERRF | (Orphanet:551) |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY | (OMIM:613668) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 | (OMIM:253280) |
Maternal hyperthermia induced birth defects | (Orphanet:2216) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Microduplication Xp11.22-p11.23 syndrome | (Orphanet:217377) |
Microlissencephaly - micromelia | (Orphanet:50810) |
Mikati-Najjar-Sahli syndrome | (Orphanet:2558) |
Miller-Dieker syndrome | (Orphanet:531) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Moynahan syndrome | (Orphanet:2574) |
Mucolipidosis type 4 | (Orphanet:578) |
Muscle-eye-brain disease | (Orphanet:588) |
Nasu-Hakola disease | (Orphanet:2770) |
Neonatal adrenoleukodystrophy | (Orphanet:44) |
Neurocutaneous melanocytosis | (Orphanet:2481) |
Neurofaciodigitorenal syndrome | (Orphanet:2673) |
Neuronal ceroid lipofuscinosis | (Orphanet:216) |
Neuronal intranuclear inclusion disease | (Orphanet:2289) |
Nodular neuronal heterotopia | (Orphanet:2149) |
Norrie disease | (Orphanet:649) |
Occipital pachygyria and polymicrogyria | (Orphanet:280640) |
Oculocerebral hypopigmentation syndrome, Cross type | (Orphanet:2719) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Odontotrichomelic syndrome | (Orphanet:2723) |
Olivopontocerebellar atrophy - deafness | (Orphanet:2732) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
Orofaciodigital syndrome type 3 | (Orphanet:2752) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
PEHO syndrome | (Orphanet:2836) |
PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM | (OMIM:614501) |
Paroxysmal exertion-induced dyskinesia | (Orphanet:98811) |
Partington syndrome | (Orphanet:94083) |
Pelizaeus-Merzbacher-like disease | (Orphanet:280270) |
Pelizaeus-Merzbacher-like due to AIMP1 mutation | (Orphanet:280293) |
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis | (Orphanet:65288) |
Peroxisomal acyl-CoA oxidase deficiency | (Orphanet:2971) |
Phakomatosis pigmentovascularis | (Orphanet:2875) |
Phosphoenolpyruvate carboxykinase 1 deficiency | (Orphanet:79316) |
Pierson syndrome | (Orphanet:2670) |
Primary cutis verticis gyrata | (Orphanet:671) |
Progressive epilepsy-intellectual deficit, Finnish type | (Orphanet:1947) |
Proximal 16p11.2 microdeletion syndrome | (Orphanet:261197) |
Pyridoxine-dependent epilepsy | (Orphanet:3006) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |
Qazi-Markouizos syndrome | (Orphanet:3010) |
RETT SYNDROME, CONGENITAL VARIANT | (OMIM:613454) |
Reading seizures | (Orphanet:166433) |
Renal tubulopathy - encephalopathy - liver failure | (Orphanet:254902) |
Rett syndrome | (Orphanet:778) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
SCHIZOPHRENIA | (OMIM:181500) |
Saccharopinuria | (Orphanet:3124) |
Schizencephaly | (Orphanet:799) |
Severe Canavan disease | (Orphanet:314911) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Severe neonatal-onset encephalopathy with microcephaly | (Orphanet:209370) |
Shoulder and girdle defects - familial intellectual deficit | (Orphanet:2580) |
Sialidosis type 1 | (Orphanet:812) |
Sinus node disease and myopia | (OMIM:182190) |
Skeletal dysplasia - epilepsy - short stature | (Orphanet:1858) |
Smith-Magenis syndrome | (Orphanet:819) |
Sotos syndrome | (Orphanet:821) |
Spastic paraplegia - facial-cutaneous lesions | (Orphanet:2819) |
Symmetrical thalamic calcifications | (Orphanet:1314) |
Tay-Sachs disease | (Orphanet:845) |
Thyrocerebrorenal syndrome | (Orphanet:3327) |
Trigonocephaly - short stature - developmental delay | (Orphanet:3369) |
Tuberous sclerosis | (Orphanet:805) |
Vici syndrome | (Orphanet:1493) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
Worster-Drought syndrome | (Orphanet:3465) |
Xeroderma pigmentosum | (Orphanet:910) |
Zellweger syndrome | (Orphanet:912) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |