disease_id,umls_name,mesh_id,mesh_name,proteins
C0002622,Amnesia,D000647,Amnesia,SIGMAR1;HRH3;GNAI1;GNAI3;APP;IL1A;IL6;NGF;POMC;PREP;TRH
C0002624,"Retrograde Amnesia",D000648,"Amnesia, Retrograde",PREP
C0003635,Apraxias,D001072,Apraxias,FOXP2
C0004310,"Auditory Perceptual Disorders",D001308,"Auditory Perceptual Disorders",CHRNA7
C0011570,"Mental Depression",D003863,Depression,RORA
C0018524,Hallucinations,D006212,Hallucinations,HOMER1
C0020796,"Profound Mental Retardation",D008607,"Intellectual Disability",MTR
C0023380,Lethargy,D053609,Lethargy,ABAT;IL1B
C0025261,"Memory Disorders",D008569,"Memory Disorders",SIGMAR1;HRH3;CHRNA7;DRD2;GABRA5;GIT1;HTR7;IGF2;APP;IL1B;INS;LNPEP;MAPT;MDK;MIF;NQO2;PARK2;PSEN1;BCL2;REL;STAT3;VEGFA
C0033922,"Psychomotor Disorders",D011596,"Psychomotor Disorders",ABAT;FOLR1
C0086132,"Depressive Symptoms",D003863,Depression,PARVA
C0349464,"Wernicke-Korsakoff Syndrome",D020915,"Korsakoff Syndrome",TKT
C0525041,"Neurobehavioral Manifestations",D019954,"Neurobehavioral Manifestations",CHRNA7;FKBP5;NGF
C0750927,"Apraxia, Developmental Verbal",D001072,Apraxias,FOXP2
C3714756,"Intellectual Disability",D008607,"Intellectual Disability",FRY;CHL1;ASCC3;CAPN10;ERLIN2;MAN1B1;C12orf57;ZNF526;RAB39B;SLC31A1;PTCHD1;PARP1;CCBE1;ADRA2B;DYNC1H1;EEF1B2;FASN;FGFR2;FOXG1;CIC;FMR1;FOLR1;GNAS;WDR62;HEXA;APC;NDST1;INPP4A;LETM1;MEF2C;ASCL1;NAGLU;SCAPER;LARP7;PMM2;TMCO1;AHI1;GON4L;LINS1;BBS7;RABL6;POLR3B;INPP5E;PTEN;RALGDS;KDM5A;RGS7;BDNF;SC5D;TMEM135;SLC2A1;TH;VRK1;YY1;CA8;COL18A1;DOCK8;MFSD2A;PRKRA;SYNGAP1;CCNA2;CACNA1G;NRXN1;HDAC4;ZBTB40