Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hallucinations	[NCBI]

Gene	Link	Information Gain
HAR1A	[NCBI]	0.000362052
MS	[NCBI]	0.000300782
CCKAR	[NCBI]	9.18755e-05
APOE	[NCBI]	3.88808e-05
CCKBR	[NCBI]	3.20072e-05
HLA-DQB1	[NCBI]	3.11636e-05
FOXP2	[NCBI]	2.92257e-05
DRD3	[NCBI]	2.73684e-05
CCK	[NCBI]	2.09814e-05
SLC6A3	[NCBI]	2.06822e-05
LGI1	[NCBI]	1.85415e-05
COMT	[NCBI]	1.74426e-05
SLC6A4	[NCBI]	1.66851e-05
SNCA	[NCBI]	1.51176e-05
HTR2A	[NCBI]	1.49428e-05
TOR1B	[NCBI]	1.1322e-05
NQO2	[NCBI]	1.03125e-05
PRL	[NCBI]	9.79428e-06
NHLRC1	[NCBI]	9.2215e-06
DRD1	[NCBI]	8.38697e-06
DRD5	[NCBI]	8.30638e-06
ALDH5A1	[NCBI]	7.95219e-06
NSD1	[NCBI]	7.60605e-06
DISC1	[NCBI]	7.40909e-06
TOR1A	[NCBI]	5.72593e-06
NOTCH3	[NCBI]	5.62601e-06
DRD2	[NCBI]	5.38559e-06
NQO1	[NCBI]	5.08561e-06
GDNF	[NCBI]	4.86723e-06
PMP22	[NCBI]	4.46174e-06
PSEN2	[NCBI]	4.28794e-06
MAPT	[NCBI]	3.95001e-06
PARK2	[NCBI]	3.80328e-06
FMR1	[NCBI]	3.36564e-06
GSTM1	[NCBI]	3.24109e-06
TH	[NCBI]	2.67616e-06
ACHE	[NCBI]	2.63647e-06
VEGFA	[NCBI]	1.65225e-06

OMIM	Link	Information gain
epilepsy, nocturnal frontal lobe, type 2	[NCBI]	0.00098052
PD	[NCBI]	0.000858292
restless legs syndrome, susceptibility to, 1	[NCBI]	0.000685
AD	[NCBI]	0.000247024
ADLTE	[NCBI]	0.000149981
NRCLP1	[NCBI]	0.000122315
COMT	[NCBI]	9.00291e-05
lujan-fryns syndrome	[NCBI]	7.36995e-05
epilepsy, nocturnal frontal lobe, type 1	[NCBI]	7.16763e-05
APOE	[NCBI]	6.82835e-05
HTR2C	[NCBI]	6.03335e-05
CCK	[NCBI]	5.89043e-05
hartnup disorder	[NCBI]	5.83004e-05
DLB	[NCBI]	5.7498e-05
HTR2A	[NCBI]	5.60027e-05
SLC6A3	[NCBI]	5.45271e-05
alzheimer disease 3	[NCBI]	5.22232e-05
LGI1	[NCBI]	5.1408e-05
DISC1	[NCBI]	4.94169e-05
DRPLA	[NCBI]	4.72646e-05
SCZD	[NCBI]	4.02885e-05
PRL	[NCBI]	3.39607e-05
FTD	[NCBI]	3.26667e-05
PSEN1	[NCBI]	2.81054e-05
DRPLA	[NCBI]	2.59757e-05
HD	[NCBI]	1.37922e-05
SLE	[NCBI]	1.35418e-05
temporal arteritis	[NCBI]	1.06419e-05
TH	[NCBI]	8.07039e-06
ACHE	[NCBI]	8.03304e-06
panencephalitis, subacute sclerosing	[NCBI]	7.2105e-06
CJD	[NCBI]	2.01209e-06