Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Inappropriate ADH Syndrome [NCBI]


Gene


Gene Link Information
Gain
01
AVP [NCBI] 0.000516419
MS [NCBI] 0.000158514
AQP2 [NCBI] 0.000105598
AVPR2 [NCBI] 4.03502e-05
NFAT5 [NCBI] 9.88476e-06
SLC12A1 [NCBI] 6.80706e-06
CLCN1 [NCBI] 6.72537e-06
PKD1 [NCBI] 3.89998e-06
PTH [NCBI] 3.22135e-06
PTHLH [NCBI] 2.83803e-06
SNCA [NCBI] 2.79188e-06
TH [NCBI] 2.28892e-06
IL6 [NCBI] 2.23254e-06
NOS3 [NCBI] 2.11773e-06




OMIM


OMIM Link Information
gain
01
AVP [NCBI] 0.00547078
NSIAD [NCBI] 0.000399126
AQP2 [NCBI] 9.6722e-05
bartter syndrome, infantile, with sensorineural deafness [NCBI] 9.2927e-05
AVPR2 [NCBI] 6.36009e-05
BPES [NCBI] 6.26044e-05
SLE [NCBI] 4.78994e-05
bsnd gene [NCBI] 4.45891e-05
CJD [NCBI] 1.64302e-05
NPPA [NCBI] 6.15755e-06
PTH [NCBI] 4.24674e-06
PTHLH [NCBI] 2.25286e-06
TH [NCBI] 1.6355e-07
RA [NCBI] 1.09971e-08




Database Center for Life Science