Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Betaine	[NCBI]

Gene	Link	Information Gain
SLC6A12	[NCBI]	0.000136873
BHMT	[NCBI]	4.42738e-05
SLC5A3	[NCBI]	2.96703e-05
SLC6A6	[NCBI]	1.69011e-05
SLC22A5	[NCBI]	6.39705e-06
BHMT2	[NCBI]	4.45521e-06
BBOX1	[NCBI]	4.34747e-06
MTHFR	[NCBI]	4.23071e-06
CBLC	[NCBI]	3.92948e-06
NFAT5	[NCBI]	3.48576e-06
CHDH	[NCBI]	2.17249e-06
ALDH9A1	[NCBI]	1.99923e-06
MMACHC	[NCBI]	1.93197e-06
SLC36A1	[NCBI]	1.75154e-06
AGXT	[NCBI]	1.63159e-06
FUS	[NCBI]	1.61293e-06
NAGS	[NCBI]	1.55389e-06
PEMT	[NCBI]	1.50557e-06
CAT	[NCBI]	1.49121e-06
SLC6A1	[NCBI]	1.40335e-06
SLC22A4	[NCBI]	1.37977e-06
PHOX2B	[NCBI]	1.24802e-06
CBS	[NCBI]	1.23029e-06
MTRR	[NCBI]	1.21501e-06
AGXT2L1	[NCBI]	1.21501e-06
ATXN3	[NCBI]	1.15815e-06
CFTR	[NCBI]	1.15597e-06
CFH	[NCBI]	1.14957e-06
AXIN1	[NCBI]	1.10238e-06
PRNP	[NCBI]	9.79186e-07
MECP2	[NCBI]	9.62589e-07
RELN	[NCBI]	9.46005e-07
ADIPOQ	[NCBI]	9.38327e-07
RET	[NCBI]	8.9247e-07
SLC6A4	[NCBI]	6.53272e-07
AVP	[NCBI]	4.64561e-07
CASP3	[NCBI]	3.44941e-07

OMIM	Link	Information gain
methylmalonic aciduria and homocystinuria, cblc type	[NCBI]	0.000386169
BHMT	[NCBI]	0.000315847
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity	[NCBI]	0.000204401
CDSP	[NCBI]	0.000197699
homocystinuria	[NCBI]	0.000134368
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type	[NCBI]	0.000128995
SLC6A12	[NCBI]	8.69157e-05
SLC6A6	[NCBI]	8.66139e-05
MJD	[NCBI]	6.06496e-05
BHMT2	[NCBI]	4.84839e-05
polycystic kidneys	[NCBI]	4.63859e-05
MTHFR	[NCBI]	4.63243e-05
AKR1B1	[NCBI]	3.24323e-05
MTRR	[NCBI]	3.16771e-05
AGXT	[NCBI]	2.81278e-05
PIAS1	[NCBI]	2.58018e-05
SLC22A5	[NCBI]	2.5208e-05
RELN	[NCBI]	2.24841e-05
TNFRSF1A	[NCBI]	1.87185e-05
CAT	[NCBI]	1.25723e-05
RA	[NCBI]	1.25e-05
AD	[NCBI]	9.52347e-06
CFTR	[NCBI]	3.68704e-06
AVP	[NCBI]	1.06658e-06
CF	[NCBI]	8.01594e-12