Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Alkalies	[NCBI]

Gene	Link	Information Gain
SLC9A3	[NCBI]	4.55688e-06
EGF	[NCBI]	4.19681e-06
PCNA	[NCBI]	2.94329e-06
ACER1	[NCBI]	2.15614e-06
CHAT	[NCBI]	2.03463e-06
SLC16A7	[NCBI]	2.03364e-06
HMMR	[NCBI]	1.95804e-06
MPG	[NCBI]	1.82472e-06
SLC13A2	[NCBI]	1.8149e-06
PDCD6IP	[NCBI]	1.70248e-06
CFTR	[NCBI]	1.66769e-06
MTF1	[NCBI]	1.56655e-06
SLC9A1	[NCBI]	1.55905e-06
VCAN	[NCBI]	1.38568e-06
KCNJ8	[NCBI]	1.34049e-06
TGFBI	[NCBI]	1.33968e-06
FGF2	[NCBI]	1.2738e-06
BID	[NCBI]	1.23657e-06
SNAI2	[NCBI]	1.23057e-06
CHGA	[NCBI]	1.2295e-06
MAPK14	[NCBI]	1.22418e-06
IBSP	[NCBI]	1.18194e-06
NOG	[NCBI]	1.16626e-06
APP	[NCBI]	1.11594e-06
SLC2A1	[NCBI]	1.09639e-06
TTR	[NCBI]	1.09509e-06
CYP2C9	[NCBI]	1.0204e-06
G6PD	[NCBI]	9.94225e-07
DHFR	[NCBI]	9.39668e-07
CAT	[NCBI]	8.18526e-07
VEGFA	[NCBI]	7.3023e-07
PTH	[NCBI]	5.70455e-07
NGF	[NCBI]	5.57958e-07
TNF	[NCBI]	3.79099e-07

OMIM	Link	Information gain
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation	[NCBI]	0.000328328
renal tubular acidosis, proximal	[NCBI]	0.000174453
renal tubular acidosis, distal, autosomal dominant	[NCBI]	0.000134519
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency	[NCBI]	0.000105446
CF	[NCBI]	6.39269e-05
CATSPER1	[NCBI]	3.91851e-05
CJD	[NCBI]	3.53674e-05
MMP1	[NCBI]	2.59467e-05
MAPK3	[NCBI]	2.11535e-05
EGF	[NCBI]	2.08231e-05
PCNA	[NCBI]	2.00173e-05
FGF2	[NCBI]	1.69434e-05
CFTR	[NCBI]	1.53896e-05
CHAT	[NCBI]	1.43713e-05
TTR	[NCBI]	8.5299e-06
HBB	[NCBI]	7.45523e-06
VEGF	[NCBI]	6.86115e-06
G6PD	[NCBI]	6.23449e-06
DHFR	[NCBI]	5.84615e-06
CAT	[NCBI]	3.90483e-06
PTH	[NCBI]	6.44534e-07
NGFB	[NCBI]	4.92904e-07
TNF	[NCBI]	3.36576e-08