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{"sheet":"VALIDATION","index":0,"n_rows":37,"n_cols":9,"rows_kept":37,"cut":false,"hidden":false,"merged":[[0,1,0,8],[1,2,1,3],[1,5,1,8]]}
[null,"SO02.DOC1274.V2018-04-03.SEC11.T79.PAPERID8881867\n8881867 - A new variant of type IV glycogenosis with primary cardiac manifestation and complete branching enzyme deficiency. In vivo detection by heart muscle biopsy.\nDISEASE: DIS005957 - Glycogen storage disease type IV"]
[null,"WIKIPEDIA TERMS","METAMAP TERMS",null,"TVP VALIDATION","DISNET VALIDATION"]
[null,"NAME","NAME","SEMANTIC TYPES","VALIDATED","WIKIPEDIA","METAMAP","TVP","RELEVANT"]
[1,"muscular, atrophy","Muscular atrophy","[patf]",true,"YES","YES","YES","YES"]
[2,"hepatosplenomegaly","Hepatosplenomegaly","[sosy]",true,"YES","YES","YES","YES"]
[3,"biopsies","Biopsy","[diap]",true,"YES","YES","YES","YES"]
[4,"peripheral, oedema","Peripheral edema","[fndg]",true,"YES","YES","YES","YES"]
[5,"hepatic, cirrhosis","Cirrhosis of liver NOS","[dsyn]",true,"YES","YES","YES","YES"]
[6,"heart, failure","Heart failure","[dsyn]",true,"YES","YES","YES","YES"]
[7,"autopsy","Autopsy","[diap]",true,"YES","YES","YES","YES"]
[8,"myopathy","Myopathy","[dsyn]",true,"YES","YES","YES","YES"]
[9,"ascites","Ascites","[fndg]",true,"YES","YES","YES","YES"]
[10,"deficiency","Malnutrition","[dsyn]",true,"YES","YES","YES","FPREAL"]
[11,"sudden, cardiac, death","Sudden cardiac death","[patf]",false,"YES","YES","NO","YES"]
[12,"disease","Disease","[dsyn]",false,"YES","YES","NO","NO"]
[13,"alive","Alive (finding)","[fndg]",false,"YES","YES","NO","NO"]
[14,"congenital, disorder","Congenital disorder","[cgab, dsyn]",false,"YES","YES","NO","NO"]
[15,"clinical, findings","Clinical finding","[sosy]",false,"YES","YES","NO","NO"]
[16,"differential, diagnosis","Differential diagnosis","[diap]",false,"YES","YES","NO","NO"]
[17,"suffer","Suffering","[mobd]",false,"YES","YES","NO","NO"]
[18,"muscle, biopsy","Biopsy of muscle NOS","[diap]",false,"YES","YES","NO","YES"]
[19,"hepatic, failure","Liver failure NOS","[dsyn]",false,"YES","YES","NO","YES"]
[20,"inherited, disorder","Hereditary disease","[dsyn]",false,"YES","YES","NO","NO"]
[21,"type, iv, glycogenosis","Glycogen storage disease, type IV","[dsyn]",false,"YES","YES","NO","NO"]
[22,"dilated, cardiomyopathy, congestive","Dilated cardiomyopathy","[dsyn]",false,"YES","YES","NO","NO"]
[23,"gastrointestinal, symptoms","Gastrointestinal symptom","[sosy]",false,"YES","YES","NO","YES"]
[]
[null,"non-specific gastrointestinal symptoms",null,null,null,"YES","NO","NO","FN"]
[null,"progressive hepatic failure",null,null,null,"YES","NO","NO","FN"]
[null,"myopathy of the heart and skeletal muscle",null,null,null,"YES","NO","NO","FN"]
[null,"progressive dilated cardiomyopathy",null,null,null,"YES","NO","NO","FN"]
[null,"Right heart and skeletal muscle biopsies",null,null,null,"YES","NO","NO","FN"]
[null,"massive accumulation of polyglucosan bodies",null,null,null,"YES","NO","NO","FN"]
[null,"complete branching enzyme deficiency",null,null,null,"YES","NO","NO","FN"]
[null,"mild dilated cardiomyopathy",null,null,null,"YES","NO","NO","FN"]
[null,"polyglucosan body myopathy",null,null,null,"YES","NO","NO","FN"]
[null,"congestive cardiomyopathy",null,null,null,"YES","NO","NO","FN"]