Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Cosyntropin	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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