Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 1106
  • Symbol: CHD2
  • Description: chromodomain helicase DNA binding protein 2

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Disease_Term Source Rank Other Values
Epileptic encephalopathy, childhood-onset, 615369 (3) OMIM high
  • Genome region : 15q26.1
  • OMIM_ID : 602119 OMIM gene ID
  • OMIM_ID : 615369 OMIM phenotype ID
Amyotrophic lateral sclerosis (sporadic) GWAS high