|
OMIM |
Link |
Information gain |
01 |
|
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
|
|