|
OMIM |
Link |
Information
gain |
01 |
|
|
folic acid, transport defect involving
|
[NCBI]
|
0.00282758
|
|
|
|
TRMA
|
[NCBI]
|
0.000714775
|
|
|
|
CDAN2
|
[NCBI]
|
0.000567689
|
|
|
|
OD
|
[NCBI]
|
0.000553188
|
|
|
|
megaloblastic anemia 1
|
[NCBI]
|
0.000424895
|
|
|
|
transcobalamin ii deficiency
|
[NCBI]
|
0.000323552
|
|
|
|
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type
|
[NCBI]
|
0.000312185
|
|
|
|
orotic aciduria i
|
[NCBI]
|
0.000261359
|
|
|
|
IFD
|
[NCBI]
|
0.000174719
|
|
|
|
DBA
|
[NCBI]
|
0.000162034
|
|
|
|
anemia, dyserythropoietic congenital, type i
|
[NCBI]
|
0.000157517
|
|
|
|
macrocytosis, familial
|
[NCBI]
|
0.000129339
|
|
|
|
waardenburg syndrome, type iid
|
[NCBI]
|
0.000106872
|
|
|
|
orotic aciduria ii
|
[NCBI]
|
9.83952e-05
|
|
|
|
MTR
|
[NCBI]
|
8.70782e-05
|
|
|
|
methylcobalamin deficiency, cblg type
|
[NCBI]
|
7.84898e-05
|
|
|
|
formiminotransferase deficiency
|
[NCBI]
|
7.66903e-05
|
|
|
|
PBT
|
[NCBI]
|
7.22548e-05
|
|
|
|
SNAI2
|
[NCBI]
|
6.52957e-05
|
|
|
|
CDAN1
|
[NCBI]
|
6.27854e-05
|
|
|
|
faciogenital dysplasia
|
[NCBI]
|
5.78898e-05
|
|
|
|
MTHFD1
|
[NCBI]
|
5.76986e-05
|
|
|
|
pyruvate decarboxylase deficiency
|
[NCBI]
|
5.22052e-05
|
|
|
|
WFS1
|
[NCBI]
|
5.14874e-05
|
|
|
|
GATA1
|
[NCBI]
|
4.67926e-05
|
|
|
|
maple syrup urine disease
|
[NCBI]
|
4.59344e-05
|
|
|
|
anemia, sideroblastic, x-linked
|
[NCBI]
|
4.17357e-05
|
|
|
|
KCNQ1
|
[NCBI]
|
3.86021e-05
|
|
|
|
GPI
|
[NCBI]
|
2.65926e-05
|
|
|
|
DHFR
|
[NCBI]
|
1.66806e-05
|
|
|
|
HBB
|
[NCBI]
|
1.48424e-05
|
|
|
|
CF
|
[NCBI]
|
7.21974e-06
|
|
|
|
HGF
|
[NCBI]
|
7.0448e-06
|
|
|
|
EPO
|
[NCBI]
|
4.21476e-06
|
|
|
|
MG
|
[NCBI]
|
2.58113e-06
|
|
|
|
CEACAM5
|
[NCBI]
|
1.03925e-06
|
|
