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ONTOLOGY REPORT - ANNOTATIONS


Term:Lennox-Gastaut syndrome
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Accession:DOID:0050561 term browser browse the term
Definition:A childhood electroclinical syndrome that is characterized by frequent seizures and intellectual disability that present in early childhood. (DO)
Synonyms:exact_synonym: Epileptic Encephalopathy, Lennox-Gastaut Type;   Lennox Gastaut Syndromes;   Lennox syndrome;   childhood epileptic encephalopathy with diffuse slow spikes and waves;   macrocephaly and epileptic encephalopathy
 primary_id: MESH:D065768
 alt_id: MESH:C535500;   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 Gabrg2 gamma-aminobutyric acid type A receptor subunit gamma 2 JBrowse link 10 27,090,913 27,179,786 RGD:8554872
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

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16017
    Developmental Diseases 9307
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8132
        genetic disease 7652
          Lennox-Gastaut syndrome 7
Path 2
Term Annotations click to browse term
  disease 16017
    disease of anatomical entity 15273
      nervous system disease 10762
        central nervous system disease 8856
          brain disease 8144
            epilepsy 1342
              electroclinical syndrome 383
                absence epilepsy 109
                  childhood electroclinical syndrome 76
                    Lennox-Gastaut syndrome 7
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.