Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Homocystinuria	[NCBI]

Gene	Link	Information Gain
CBS	[NCBI]	0.000577446
MMACHC	[NCBI]	0.000135889
MTRR	[NCBI]	6.36097e-05
FBN1	[NCBI]	2.3866e-05
MTR	[NCBI]	2.25344e-05
MTHFR	[NCBI]	1.76594e-05
C2orf25	[NCBI]	1.59993e-05
CBLC	[NCBI]	1.10705e-05
MAT1A	[NCBI]	1.00904e-05
NAGS	[NCBI]	8.72467e-06
CST3	[NCBI]	8.10649e-06
NOTCH1	[NCBI]	4.65204e-06
PAH	[NCBI]	4.18649e-06
HTT	[NCBI]	2.99023e-06
SOD1	[NCBI]	2.39949e-06
ACHE	[NCBI]	2.18853e-06

OMIM	Link	Information gain
homocystinuria	[NCBI]	0.00586721
methylmalonic aciduria and homocystinuria, cbld type	[NCBI]	0.00372806
methylmalonic aciduria and homocystinuria, cblc type	[NCBI]	0.00138371
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity	[NCBI]	0.00113232
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type	[NCBI]	0.000873328
methylcobalamin deficiency, cblg type	[NCBI]	0.000396443
homocysteinemia	[NCBI]	0.000305856
MTHFR	[NCBI]	0.000287196
MFS	[NCBI]	0.000165465
MTRR	[NCBI]	0.000165289
MTR	[NCBI]	0.000141717
puerto rican infant hypotonia syndrome	[NCBI]	0.000101119
sulfocysteinuria	[NCBI]	7.70927e-05
mmachc gene	[NCBI]	7.25207e-05
neural tube defects, folate-sensitive	[NCBI]	6.11102e-05
transcobalamin ii deficiency	[NCBI]	3.1778e-05
contractural arachnodactyly, congenital	[NCBI]	2.70623e-05
ACHE	[NCBI]	8.15255e-08