Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Perceptual Disorders	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	0.000422765
APOE	[NCBI]	1.83355e-05
CTNS	[NCBI]	1.0971e-05
LGI1	[NCBI]	1.09366e-05
GRN	[NCBI]	9.48789e-06
NRG1	[NCBI]	9.34784e-06
DBH	[NCBI]	9.15715e-06
SLC6A3	[NCBI]	7.85657e-06
MAPT	[NCBI]	6.78688e-06
BDNF	[NCBI]	5.52206e-06
TH	[NCBI]	5.44884e-06
GFAP	[NCBI]	4.5053e-06

OMIM	Link	Information gain
tune deafness	[NCBI]	0.00107364
prosopagnosia, hereditary	[NCBI]	0.00098052
AD	[NCBI]	0.000429662
FTD	[NCBI]	9.64138e-05
musical perfect pitch	[NCBI]	8.63791e-05
muckle-wells syndrome	[NCBI]	7.23176e-05
ADHD	[NCBI]	5.36411e-05
NRG1	[NCBI]	5.15494e-05
APOE	[NCBI]	4.82481e-05
PD	[NCBI]	4.14955e-05
GDNF	[NCBI]	2.93524e-05
MJD	[NCBI]	2.76451e-05
BDNF	[NCBI]	2.16928e-05
GTS	[NCBI]	2.10017e-05
TH	[NCBI]	2.05902e-05
GFAP	[NCBI]	1.56487e-05
panencephalitis, subacute sclerosing	[NCBI]	1.50924e-05
PWS	[NCBI]	1.3906e-05
CJD	[NCBI]	7.94684e-06