Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Perceptual Disorders [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science