ONTOLOGY REPORT - ANNOTATIONS


Term:Lennox-Gastaut syndrome
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Accession:DOID:0050561 term browser browse the term
Definition:A childhood-onset epilepsy syndrome.
Synonyms:exact_synonym: Childhood Epileptic Encephalopathy with Diffuse Slow Spikes and Waves;   Epileptic Encephalopathy, Lennox-Gastaut Type;   Lennox Gastaut Syndromes;   Lennox syndrome;   MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY
 primary_id: MESH:C535500;   MESH:D065768;   RDO:0000642;   RDO:0015946
 alt_id: DOID:9003320;   OMIM:606369
 xref: GARD:9912;   ORDO:2382
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Lennox-Gastaut syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dgkd diacylglycerol kinase, delta JBrowse link 9 94,980,328 95,071,531 RGD:13592920
G Gatm glycine amidinotransferase JBrowse link 3 114,711,570 114,728,155 RGD:8554872
G Mapk10 mitogen activated protein kinase 10 JBrowse link 14 8,079,955 8,371,508 RGD:8554872
G Polg DNA polymerase gamma, catalytic subunit JBrowse link 1 141,172,117 141,188,893 RGD:8554872
G Scn1a sodium voltage-gated channel alpha subunit 1 JBrowse link 3 52,388,811 52,533,365 RGD:8554872
G Zeb2 zinc finger E-box binding homeobox 2 JBrowse link 3 29,857,289 29,985,932 RGD:8554872

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Path 1
Term Annotations click to browse term
  disease 14875
    Developmental Diseases 7711
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6750
        genetic disease 5997
          Lennox-Gastaut syndrome 6
Path 2
Term Annotations click to browse term
  disease 14875
    disease of anatomical entity 14051
      nervous system disease 9116
        central nervous system disease 6913
          brain disease 6418
            epilepsy 1017
              electroclinical syndrome 282
                absence epilepsy 95
                  childhood electroclinical syndrome 73
                    Lennox-Gastaut syndrome 6
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.