report-2,,,,,,,,,,,,,,,
DS_ID,GENE_SYMBOL,DSI,DPI,UMLS,DISEASE_NAME,DISEASE_TYPE,DISEASE_CLASS,DISEASE_SEMANTIC_TYPE,SCORE,EI,YEAR_INITIAL,YEAR_FINAL,NUM_OF_PMIDS,NUM_OF_SNPS,SOURCE_DATABASE
,FOXG1,0.522,0.692,C2748910,"Rett Syndrome, Atypical",disease,C16;C10,Disease or Syndrome,0.34,1,2008,2019,3,0,ORPHANET
,EGR2,0.547,0.769,C0035372,Rett Syndrome,disease,C16;C10,Disease or Syndrome,0.31,1,2009,2009,1,0,CTD_human
,MECP2,0.414,0.846,C0035372,Rett Syndrome,disease,C16;C10,Disease or Syndrome,1,0.977,1975,2020,50,335,CLINGEN;CTD_human;GENOMICS_ENGLAND;UNIPROT
,PTPN1,0.523,0.731,C0035372,Rett Syndrome,disease,C16;C10,Disease or Syndrome,0.3,1,2015,2015,1,0,CTD_human
,CDKL5,0.522,0.692,C0035372,Rett Syndrome,disease,C16;C10,Disease or Syndrome,0.5,0.962,2004,2019,1,2,CTD_human
,CDKL5,0.522,0.692,C2748910,"Rett Syndrome, Atypical",disease,C16;C10,Disease or Syndrome,0.5,0.923,2008,2019,1,41,ORPHANET
,STXBP1,0.532,0.692,C2748910,"Rett Syndrome, Atypical",disease,C16;C10,Disease or Syndrome,0.3,1,2015,2015,2,0,ORPHANET
,NTNG1,0.65,0.423,C2748910,"Rett Syndrome, Atypical",disease,C16;C10,Disease or Syndrome,0.31,1,2007,2007,1,0,ORPHANET
,GABBR2,0.65,0.538,C0035372,Rett Syndrome,disease,C16;C10,Disease or Syndrome,0.41,1,2017,2018,2,1,GENOMICS_ENGLAND
,GABBR2,0.65,0.538,C2748910,"Rett Syndrome, Atypical",disease,C16;C10,Disease or Syndrome,0.3,1,2017,2017,1,0,ORPHANET