|
OMIM |
Link |
Information gain |
01 |
|
methylmalonic aciduria and homocystinuria, cblf type
|
[NCBI]
|
0.0113399
|
|
|
methylmalonic aciduria and homocystinuria, cbld type
|
[NCBI]
|
0.00754708
|
|
|
r binder deficiency with lactoferrin deficiency
|
[NCBI]
|
0.00337314
|
|
|
methylmalonic aciduria and homocystinuria, cblc type
|
[NCBI]
|
0.0022489
|
|
|
megaloblastic anemia 1
|
[NCBI]
|
0.00184571
|
|
|
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency
|
[NCBI]
|
0.00120536
|
|
|
methylcobalamin deficiency, cblg type
|
[NCBI]
|
0.00118069
|
|
|
IFD
|
[NCBI]
|
0.00107206
|
|
|
folic acid, transport defect involving
|
[NCBI]
|
0.0010616
|
|
|
methylmalonic aciduria, cbla type
|
[NCBI]
|
0.000835692
|
|
|
MTR
|
[NCBI]
|
0.000824973
|
|
|
homocysteinemia
|
[NCBI]
|
0.000693202
|
|
|
transcobalamin ii deficiency
|
[NCBI]
|
0.000608978
|
|
|
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type
|
[NCBI]
|
0.000600103
|
|
|
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity
|
[NCBI]
|
0.000434276
|
|
|
CUBN
|
[NCBI]
|
0.000406505
|
|
|
pernicious anemia
|
[NCBI]
|
0.000365572
|
|
|
methylmalonic aciduria, cblb type
|
[NCBI]
|
0.000234229
|
|
|
neural tube defects, folate-sensitive
|
[NCBI]
|
0.000232728
|
|
|
MTHFR
|
[NCBI]
|
0.000184822
|
|
|
SLE
|
[NCBI]
|
0.000129541
|
|
|
r binder protein
|
[NCBI]
|
0.000122373
|
|
|
MDD
|
[NCBI]
|
0.000113707
|
|
|
methylmalonic aciduria, cblh type
|
[NCBI]
|
0.000107228
|
|
|
MUT
|
[NCBI]
|
0.000101007
|
|
|
CF
|
[NCBI]
|
0.000100244
|
|
|
homocystinuria
|
[NCBI]
|
9.45411e-05
|
|
|
MTRR
|
[NCBI]
|
9.17119e-05
|
|
|
RA
|
[NCBI]
|
8.40507e-05
|
|
|
MMAB
|
[NCBI]
|
8.15414e-05
|
|
|
HES
|
[NCBI]
|
6.51505e-05
|
|
|
formiminotransferase deficiency
|
[NCBI]
|
6.29195e-05
|
|
|
GIF
|
[NCBI]
|
6.11009e-05
|
|
|
AD
|
[NCBI]
|
5.84972e-05
|
|
|
methionine adenosyltransferase deficiency
|
[NCBI]
|
5.1634e-05
|
|
|
TRMA
|
[NCBI]
|
5.04189e-05
|
|
|
EPO
|
[NCBI]
|
5.02675e-05
|
|
|
mmachc gene
|
[NCBI]
|
4.07506e-05
|
|
|
PD
|
[NCBI]
|
3.95825e-05
|
|
|
MMAA
|
[NCBI]
|
3.33297e-05
|
|
|
COMT
|
[NCBI]
|
3.04263e-05
|
|
|
IP
|
[NCBI]
|
2.87872e-05
|
|
|
ALAS1
|
[NCBI]
|
2.7363e-05
|
|
|
FIP1L1
|
[NCBI]
|
2.46284e-05
|
|
|
CGD
|
[NCBI]
|
2.31635e-05
|
|
|
NPAS2
|
[NCBI]
|
2.1494e-05
|
|
|
hypogonadotropic hypogonadism
|
[NCBI]
|
2.05742e-05
|
|
|
MAT1A
|
[NCBI]
|
2.04269e-05
|
|
|
PER2
|
[NCBI]
|
1.95401e-05
|
|
|
APS1
|
[NCBI]
|
1.9425e-05
|
|
|
BHMT
|
[NCBI]
|
1.90224e-05
|
|
|
GPX1
|
[NCBI]
|
1.65241e-05
|
|
|
FGF8
|
[NCBI]
|
1.21084e-05
|
|
|
DHFR
|
[NCBI]
|
1.08624e-05
|
|
|
ALB
|
[NCBI]
|
1.06622e-05
|
|
|
FPGS
|
[NCBI]
|
1.0356e-05
|
|
|
APOE
|
[NCBI]
|
1.01518e-05
|
|
|
PG
|
[NCBI]
|
9.39228e-06
|
|
|
PON1
|
[NCBI]
|
8.6557e-06
|
|
|
AGER
|
[NCBI]
|
8.18613e-06
|
|
|
EGF
|
[NCBI]
|
7.96636e-06
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
6.86858e-06
|
|
|
SERPINA6
|
[NCBI]
|
5.65221e-06
|
|
|
CD
|
[NCBI]
|
4.31028e-06
|
|
|
CP
|
[NCBI]
|
4.20631e-06
|
|
|
amyloidosis vi
|
[NCBI]
|
3.92707e-06
|
|
|
TNF
|
[NCBI]
|
3.85303e-06
|
|
|
TPO
|
[NCBI]
|
3.75693e-06
|
|
|
CRC
|
[NCBI]
|
2.6275e-06
|
|
|
ALD
|
[NCBI]
|
1.93452e-06
|
|
|
TH
|
[NCBI]
|
1.68291e-06
|
|
|
temporal arteritis
|
[NCBI]
|
1.34163e-06
|
|
|
FTD
|
[NCBI]
|
1.20911e-06
|
|
|
VIP
|
[NCBI]
|
9.61024e-07
|
|
|
TYMS
|
[NCBI]
|
7.01621e-07
|
|
|
MPO
|
[NCBI]
|
5.05379e-07
|
|
|
CAT
|
[NCBI]
|
3.32566e-08
|
|
|
F3
|
[NCBI]
|
3.27758e-08
|
|