|
OMIM |
Link |
Information gain |
01 |
|
AFP
|
[NCBI]
|
0.00226637
|
|
|
anencephaly
|
[NCBI]
|
0.00174009
|
|
|
neural tube defects, folate-sensitive
|
[NCBI]
|
0.00163475
|
|
|
THAS
|
[NCBI]
|
0.00119383
|
|
|
neural tube defects
|
[NCBI]
|
0.00110764
|
|
|
chiari malformation type ii
|
[NCBI]
|
0.000984578
|
|
|
poland syndrome
|
[NCBI]
|
0.000791272
|
|
|
ACHE
|
[NCBI]
|
0.000770467
|
|
|
dysgnathia complex
|
[NCBI]
|
0.000592366
|
|
|
exstrophy of bladder
|
[NCBI]
|
0.000592366
|
|
|
MKS2
|
[NCBI]
|
0.000561
|
|
|
GRHL3
|
[NCBI]
|
0.000505463
|
|
|
acetabular dysplasia
|
[NCBI]
|
0.000493306
|
|
|
IH
|
[NCBI]
|
0.000446614
|
|
|
MKS1
|
[NCBI]
|
0.000383959
|
|
|
VANGL2
|
[NCBI]
|
0.000350339
|
|
|
diaphragmatic hernia, congenital
|
[NCBI]
|
0.000337721
|
|
|
NLS
|
[NCBI]
|
0.000325462
|
|
|
MKS3
|
[NCBI]
|
0.000294145
|
|
|
myeloproliferative syndrome, transient
|
[NCBI]
|
0.00029399
|
|
|
MTHFR
|
[NCBI]
|
0.000262877
|
|
|
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity
|
[NCBI]
|
0.000260315
|
|
|
SHH
|
[NCBI]
|
0.00025239
|
|
|
CPI
|
[NCBI]
|
0.00020442
|
|
|
MTHFD1
|
[NCBI]
|
0.000197362
|
|
|
FOLR1
|
[NCBI]
|
0.000191043
|
|
|
MLP
|
[NCBI]
|
0.000189254
|
|
|
neural tube defects, x-linked
|
[NCBI]
|
0.000170349
|
|
|
VANGL1
|
[NCBI]
|
0.000166911
|
|
|
valproate embryopathy, susceptibility to
|
[NCBI]
|
0.000164383
|
|
|
HFM
|
[NCBI]
|
0.000162511
|
|
|
oeis complex
|
[NCBI]
|
0.000159358
|
|
|
PAX3
|
[NCBI]
|
0.000144644
|
|
|
T
|
[NCBI]
|
0.000141803
|
|
|
CITED2
|
[NCBI]
|
0.000141803
|
|
|
folate level in erythrocytes
|
[NCBI]
|
0.000115987
|
|
|
craniofacial abnormalities, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation
|
[NCBI]
|
0.000115987
|
|
|
SCDO1
|
[NCBI]
|
0.000110287
|
|
|
MTR
|
[NCBI]
|
0.000104094
|
|
|
dk phocomelia syndrome
|
[NCBI]
|
9.35273e-05
|
|
|
SCDO3
|
[NCBI]
|
9.35273e-05
|
|
|
LRP6
|
[NCBI]
|
9.27312e-05
|
|
|
TNF
|
[NCBI]
|
8.77591e-05
|
|
|
velocardiofacial syndrome
|
[NCBI]
|
8.58303e-05
|
|
|
omphalocele, diaphragmatic hernia, and radial ray defects
|
[NCBI]
|
8.50577e-05
|
|
|
coloboma, uveal, with cleft lip and palate and mental retardation
|
[NCBI]
|
8.50577e-05
|
|
|
SKI
|
[NCBI]
|
8.45865e-05
|
|
|
ZIC3
|
[NCBI]
|
7.65258e-05
|
|
|
aprosencephaly syndrome
|
[NCBI]
|
7.54786e-05
|
|
|
goldberg-shprintzen megacolon syndrome
|
[NCBI]
|
6.95252e-05
|
|
|
gastroschisis
|
[NCBI]
|
6.72141e-05
|
|
|
monosomy 7 of bone marrow
|
[NCBI]
|
6.34027e-05
|
|
|
por deficiency
|
[NCBI]
|
6.34027e-05
|
|
|
KNO
|
[NCBI]
|
6.34027e-05
|
|
|
SMARCA1
|
[NCBI]
|
6.30456e-05
|
|
|
activating molecule in beclin 1-regulated autophagy
|
[NCBI]
|
6.30456e-05
|
|
|
MAP3K4
|
[NCBI]
|
6.30456e-05
|
|
|
FOLR2
|
[NCBI]
|
6.30456e-05
|
|
|
EPHA7
|
[NCBI]
|
6.30456e-05
|
|
|
PHACTR4
|
[NCBI]
|
6.30456e-05
|
|
|
HIPK1
|
[NCBI]
|
6.30456e-05
|
|
|
SHROOM3
|
[NCBI]
|
6.30456e-05
|
|
|
KIAA0586
|
[NCBI]
|
6.30456e-05
|
|
|
omphalocele
|
[NCBI]
|
6.17915e-05
|
|
|
WS3
|
[NCBI]
|
6.03283e-05
|
|
|
wildervanck syndrome
|
[NCBI]
|
6.03283e-05
|
|
|
WZS
|
[NCBI]
|
5.89884e-05
|
|
|
hydrocephalus
|
[NCBI]
|
5.89884e-05
|
|
|
mowat-wilson syndrome
|
[NCBI]
|
5.66065e-05
|
|
|
DGS
|
[NCBI]
|
5.59523e-05
|
|
|
CFTD
|
[NCBI]
|
5.45363e-05
|
|
|
MVA
|
[NCBI]
|
5.35948e-05
|
|
|
sacral defect with anterior meningocele
|
[NCBI]
|
5.35948e-05
|
|
|
hartnup disorder
|
[NCBI]
|
5.18653e-05
|
|
|
IS1
|
[NCBI]
|
5.14555e-05
|
|
|
SLOS
|
[NCBI]
|
5.01103e-05
|
|
|
TAGLN2
|
[NCBI]
|
4.92823e-05
|
|
|
CECR2
|
[NCBI]
|
4.92823e-05
|
|
|
EFNA5
|
[NCBI]
|
4.92823e-05
|
|
|
CART1
|
[NCBI]
|
4.92823e-05
|
|
|
TXN2
|
[NCBI]
|
4.92823e-05
|
|
|
LFNG
|
[NCBI]
|
4.92823e-05
|
|
|
RAB23
|
[NCBI]
|
4.92823e-05
|
|
|
MGAT1
|
[NCBI]
|
4.92823e-05
|
|
|
NAP1L2
|
[NCBI]
|
4.92823e-05
|
|
|
TULP3
|
[NCBI]
|
4.92823e-05
|
|
|
scribble, drosophila, homolog of
|
[NCBI]
|
4.92823e-05
|
|
|
VEGF
|
[NCBI]
|
4.8214e-05
|
|
|
homocysteinemia
|
[NCBI]
|
4.52793e-05
|
|
|
PRKCB1
|
[NCBI]
|
4.40983e-05
|
|
|
MKS1
|
[NCBI]
|
4.40983e-05
|
|
|
NFIA
|
[NCBI]
|
4.40983e-05
|
|
|
JARID2
|
[NCBI]
|
4.40983e-05
|
|
|
CEACAM5
|
[NCBI]
|
4.24488e-05
|
|
|
CDH6
|
[NCBI]
|
4.0738e-05
|
|
|
TMEM67
|
[NCBI]
|
4.0738e-05
|
|
|
SIL
|
[NCBI]
|
3.82437e-05
|
|
|
MAPK9
|
[NCBI]
|
3.82437e-05
|
|
|
NHLH1
|
[NCBI]
|
3.82437e-05
|
|
|
CDH2
|
[NCBI]
|
3.62596e-05
|
|
|
XBP1
|
[NCBI]
|
3.62596e-05
|
|
|
ZIC2
|
[NCBI]
|
3.46125e-05
|
|
|
TFAP2A
|
[NCBI]
|
3.46125e-05
|
|
|
ornithine transcarbamylase deficiency, hyperammonemia due to
|
[NCBI]
|
3.42829e-05
|
|
|
WS1
|
[NCBI]
|
3.40253e-05
|
|
|
HOXA1
|
[NCBI]
|
3.3205e-05
|
|
|
SLC19A1
|
[NCBI]
|
3.3205e-05
|
|
|
BCL10
|
[NCBI]
|
3.3205e-05
|
|
|
EP300
|
[NCBI]
|
3.19767e-05
|
|
|
PAX1
|
[NCBI]
|
3.19767e-05
|
|
|
APAF1
|
[NCBI]
|
3.08874e-05
|
|
|
POR
|
[NCBI]
|
3.08874e-05
|
|
|
GADD45A
|
[NCBI]
|
2.99091e-05
|
|
|
BHMT
|
[NCBI]
|
2.99091e-05
|
|
|
MAPK8
|
[NCBI]
|
2.90216e-05
|
|
|
GATA3
|
[NCBI]
|
2.90216e-05
|
|
|
COL18A1
|
[NCBI]
|
2.90216e-05
|
|
|
PDGFRA
|
[NCBI]
|
2.67687e-05
|
|
|
GFAP
|
[NCBI]
|
2.56184e-05
|
|
|
PRKCG
|
[NCBI]
|
2.49511e-05
|
|
|
FASN
|
[NCBI]
|
2.29743e-05
|
|
|
BBS
|
[NCBI]
|
2.27839e-05
|
|
|
TERC
|
[NCBI]
|
2.25398e-05
|
|
|
transcobalamin ii deficiency
|
[NCBI]
|
2.25398e-05
|
|
|
PCNA
|
[NCBI]
|
2.13058e-05
|
|
|
JAG1
|
[NCBI]
|
1.96552e-05
|
|
|
VASP
|
[NCBI]
|
1.93519e-05
|
|
|
PGK1
|
[NCBI]
|
1.77235e-05
|
|
|
STK11
|
[NCBI]
|
1.70109e-05
|
|
|
IHH
|
[NCBI]
|
1.20252e-05
|
|
|
homocystinuria
|
[NCBI]
|
8.47856e-06
|
|
|
BCHE
|
[NCBI]
|
8.1141e-06
|
|
|
HGF
|
[NCBI]
|
7.05071e-06
|
|
|
FGFR2
|
[NCBI]
|
6.7235e-06
|
|
|
EPO
|
[NCBI]
|
6.12011e-06
|
|
|
SDC2
|
[NCBI]
|
5.93492e-06
|
|
|
PYY
|
[NCBI]
|
4.00713e-06
|
|
|
APOB
|
[NCBI]
|
3.90228e-06
|
|
|
BRCA1
|
[NCBI]
|
3.81466e-06
|
|
|
TP53
|
[NCBI]
|
3.20604e-06
|
|
|
F3
|
[NCBI]
|
2.09818e-06
|
|
|
CRC
|
[NCBI]
|
1.74472e-06
|
|
|
MUC1
|
[NCBI]
|
4.22456e-07
|
|
|
PTK2
|
[NCBI]
|
1.8389e-07
|
|
|
PTHLH
|
[NCBI]
|
6.43375e-08
|
|