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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-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
For additional species annotation, visit the Alliance of Genome Resources.


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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 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          Lennox-Gastaut syndrome 6
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        central nervous system disease 6892
          brain disease 6396
            epilepsy 1015
              electroclinical syndrome 281
                absence epilepsy 95
                  childhood electroclinical syndrome 74
                    Lennox-Gastaut syndrome 6
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