Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Cosyntropin [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.000167687
AVP [NCBI] 4.92363e-06
MC2R [NCBI] 4.40497e-06
PRL [NCBI] 4.24898e-06
LPL [NCBI] 3.72147e-06
CRH [NCBI] 3.22552e-06
SHBG [NCBI] 2.76646e-06
CYP11B1 [NCBI] 1.9746e-06
NR3C1 [NCBI] 1.41309e-06
PYY [NCBI] 1.27213e-06
POMC [NCBI] 1.18843e-06
IL6 [NCBI] 1.03146e-06
TRH [NCBI] 9.12695e-07
BDNF [NCBI] 8.61882e-07
PCNA [NCBI] 8.17021e-07
NPY [NCBI] 7.47555e-07
TNF [NCBI] 5.03189e-07



OMIM


 OMIM Link Information
gain		 01
PPNAD1 [NCBI] 0.000152301
CRH [NCBI] 0.000131222
infantile spasm syndrome, x-linked [NCBI] 0.000130894
AIMAH [NCBI] 0.000104009
SERPINA6 [NCBI] 0.000102519
GRA [NCBI] 9.3536e-05
MDD [NCBI] 3.84061e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 3.51282e-05
AVP [NCBI] 2.3054e-05
LPL [NCBI] 2.13546e-05
SHBG [NCBI] 1.78858e-05
PRL [NCBI] 1.53055e-05
ABP1 [NCBI] 1.2941e-05
PYY [NCBI] 7.68934e-06
POMC [NCBI] 6.44846e-06
RA [NCBI] 5.61983e-06
NPPA [NCBI] 2.76728e-06
BDNF [NCBI] 1.34411e-06
PCNA [NCBI] 8.34258e-07
TNF [NCBI] 7.40771e-07
CEACAM5 [NCBI] 4.97013e-07
NPY [NCBI] 2.537e-07



Database Center for Life Science