Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hydroxocobalamin	[NCBI]

Gene	Link	Information Gain
MMACHC	[NCBI]	5.52706e-06
CBLC	[NCBI]	5.19861e-06
MTRR	[NCBI]	4.07204e-06
ACADVL	[NCBI]	2.35441e-06
CFH	[NCBI]	1.77083e-06
HSPB1	[NCBI]	1.58104e-06
HMOX1	[NCBI]	1.45e-06
GJB2	[NCBI]	1.43513e-06
SLC6A4	[NCBI]	1.26776e-06
VWF	[NCBI]	1.07824e-06

OMIM	Link	Information gain
methylmalonic aciduria and homocystinuria, cbld type	[NCBI]	0.00501703
methylmalonic aciduria and homocystinuria, cblc type	[NCBI]	0.00128274
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type	[NCBI]	0.000480125
transcobalamin ii deficiency	[NCBI]	0.000121179
megaloblastic anemia 1	[NCBI]	9.79079e-05
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency	[NCBI]	9.38489e-05
MTRR	[NCBI]	4.21038e-05
MTR	[NCBI]	2.96216e-05