Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Protein Deficiency	[NCBI]

Gene	Link	Information Gain
PSAP	[NCBI]	5.15562e-05
ACHE	[NCBI]	1.6386e-05
EPO	[NCBI]	1.34364e-05
TTR	[NCBI]	1.2498e-05
CHAT	[NCBI]	1.18719e-05
SLC5A3	[NCBI]	1.0094e-05
CAT	[NCBI]	9.72054e-06
PC	[NCBI]	8.92106e-06
HAPLN1	[NCBI]	8.714e-06
WFDC5	[NCBI]	8.58009e-06
TTPA	[NCBI]	8.03365e-06
SERPING1	[NCBI]	7.77392e-06
IGFBP3	[NCBI]	6.17117e-06
PON1	[NCBI]	5.17566e-06
F2	[NCBI]	5.05952e-06
F5	[NCBI]	4.70618e-06
CETP	[NCBI]	4.31922e-06
ADA	[NCBI]	4.30704e-06
TRH	[NCBI]	3.94477e-06
LPL	[NCBI]	3.55517e-06
MBP	[NCBI]	3.2012e-06
TGFB1	[NCBI]	2.80836e-06
CDKN1A	[NCBI]	2.00851e-06
TNF	[NCBI]	8.12137e-07

OMIM	Link	Information gain
tay-sachs disease, ab variant	[NCBI]	0.000107666
enterokinase deficiency	[NCBI]	0.000105561
metachromatic leukodystrophy due to saposin b deficiency	[NCBI]	9.7782e-05
protein c deficiency, congenital thrombotic disease due to	[NCBI]	8.13856e-05
TGD	[NCBI]	7.85232e-05
HAE	[NCBI]	6.97197e-05
ABL	[NCBI]	6.94508e-05
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency	[NCBI]	6.67567e-05
TSD	[NCBI]	5.08561e-05
ACHE	[NCBI]	4.73701e-05
CD47	[NCBI]	4.49227e-05
TBG	[NCBI]	4.44511e-05
PROS1	[NCBI]	4.06731e-05
TTR	[NCBI]	3.85198e-05
CHAT	[NCBI]	3.6939e-05
PC	[NCBI]	3.56351e-05
GPT	[NCBI]	3.54495e-05
EPO	[NCBI]	3.23181e-05
PON1	[NCBI]	2.91757e-05
CAT	[NCBI]	2.60026e-05
SPINK1	[NCBI]	2.50387e-05
AVP	[NCBI]	1.87644e-05
LPL	[NCBI]	6.76066e-06
CRH	[NCBI]	5.3633e-06
MBP	[NCBI]	4.7374e-06
CF	[NCBI]	2.32532e-06
VEGF	[NCBI]	1.10356e-06
TNF	[NCBI]	5.63063e-07