loading...| Preferred Name |
Lennox-Gastaut syndrome |
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| Synonyms |
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| Definitions |
A rare, severe early-onset developmental epileptic encephalopathy characterized by the triad of intellectual impairment, multiple seizure types, and typical electroencephalography (EEG) abnormalities. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_2382 |
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| definition |
A rare, severe early-onset developmental epileptic encephalopathy characterized by the triad of intellectual impairment, multiple seizure types, and typical electroencephalography (EEG) abnormalities. |
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| definition_citation |
Orphanet |
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2382 |
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| has_age_of_onset |
Childhood Infancy |
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| has_inheritance |
Not applicable Multigenic/multifactorial Autosomal dominant |
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| hasDbXref |
OMIM:617113 OMIM:618141 ICD-10:G40.4 OMIM:616346 MeSH:D065768 OMIM:615369 UMLS:C0238111 MedDRA:10048816 ICD-11:8A62.1 |
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| label |
Lennox-Gastaut syndrome |
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| notation |
ORPHA:2382 |
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| part_of |
http://www.orpha.net/ORDO/Orphanet_98749 http://www.orpha.net/ORDO/Orphanet_98744 |
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| prefixIRI |
ORDO:Orphanet_2382 |
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| prefLabel |
Lennox-Gastaut syndrome |
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| present_in |
Europe AND has_annual_incidence_average_value : 0.1 AND has_annual_incidence_range : 1-9 / 1 000 000 Europe AND has_point_prevalence_average_value : 15.0 AND has_point_prevalence_range : 1-5 / 10 000 |
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| treeView |
http://www.orpha.net/ORDO/Orphanet_98749 http://www.orpha.net/ORDO/Orphanet_98744 |
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| subClassOf |