Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Homocystine	[NCBI]

Gene	Link	Information Gain
MTHFR	[NCBI]	1.34743e-05
VWF	[NCBI]	2.55243e-06
MTHFD1	[NCBI]	2.2067e-06
MTR	[NCBI]	1.8621e-06
CBS	[NCBI]	1.85186e-06
MTRR	[NCBI]	1.83654e-06
ACHE	[NCBI]	1.00182e-06

OMIM	Link	Information gain
homocystinuria	[NCBI]	0.000659536
homocysteinemia	[NCBI]	0.000509151
methylmalonic aciduria and homocystinuria, cblc type	[NCBI]	0.000235916
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity	[NCBI]	0.000204401
sulfocysteinuria	[NCBI]	0.000114103
cystathioninuria	[NCBI]	0.000112353
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency	[NCBI]	6.95714e-05
temporal arteritis	[NCBI]	4.253e-05
MTHFR	[NCBI]	2.16419e-05
RA	[NCBI]	1.25e-05
TNFRSF11B	[NCBI]	9.48795e-06
PPARA	[NCBI]	8.68833e-06
ACHE	[NCBI]	2.23338e-06