|
OMIM |
Link |
Information gain |
01 |
|
FRNS
|
[NCBI]
|
0.00144739
|
|
|
ACG1A
|
[NCBI]
|
0.0012838
|
|
|
urogenital adysplasia, hereditary
|
[NCBI]
|
0.00118971
|
|
|
short rib-polydactyly syndrome, type i
|
[NCBI]
|
0.00097863
|
|
|
cardiomyopathy, fatal fetal, due to myocardial calcification
|
[NCBI]
|
0.000814853
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
0.00080975
|
|
|
multiple pterygium syndrome, lethal type
|
[NCBI]
|
0.000769156
|
|
|
megacystis-microcolon-intestinal hypoperistalsis syndrome
|
[NCBI]
|
0.000740364
|
|
|
dandy-walker-like malformation with atrioventricular septal defect
|
[NCBI]
|
0.000626032
|
|
|
osteodysplasia, familial, anderson type
|
[NCBI]
|
0.00059777
|
|
|
NLS
|
[NCBI]
|
0.000544841
|
|
|
PCD
|
[NCBI]
|
0.000511773
|
|
|
holoprosencephaly
|
[NCBI]
|
0.000464399
|
|
|
campomelia, cumming type
|
[NCBI]
|
0.000463831
|
|
|
renal-hepatic-pancreatic dysplasia with dandy-walker cyst
|
[NCBI]
|
0.000463831
|
|
|
patent ductus arteriosus
|
[NCBI]
|
0.000463831
|
|
|
spondylometaphyseal dysplasia, sedaghatian type
|
[NCBI]
|
0.000424981
|
|
|
opsismodysplasia
|
[NCBI]
|
0.000424981
|
|
|
MKS2
|
[NCBI]
|
0.0003942
|
|
|
lethal congenital contracture syndrome 1
|
[NCBI]
|
0.0003942
|
|
|
metatropic dwarfism
|
[NCBI]
|
0.00036875
|
|
|
popliteal pterygium syndrome, lethal type
|
[NCBI]
|
0.000347089
|
|
|
dyssegmental dysplasia, rolland-desbuquois type
|
[NCBI]
|
0.000347089
|
|
|
RA
|
[NCBI]
|
0.000327624
|
|
|
renal hamartomas, nephroblastomatosis, and fetal gigantism
|
[NCBI]
|
0.000311633
|
|
|
AFP
|
[NCBI]
|
0.000307184
|
|
|
OFD4
|
[NCBI]
|
0.000296762
|
|
|
short rib-polydactyly syndrome, type iii
|
[NCBI]
|
0.000296762
|
|
|
SHFLD1
|
[NCBI]
|
0.000283326
|
|
|
short rib-polydactyly syndrome, type iv
|
[NCBI]
|
0.000271087
|
|
|
AMCN
|
[NCBI]
|
0.000259858
|
|
|
constricting bands, congenital
|
[NCBI]
|
0.000259858
|
|
|
SLE
|
[NCBI]
|
0.000243032
|
|
|
short rib-polydactyly syndrome, type ii
|
[NCBI]
|
0.000239884
|
|
|
gracile bone dysplasia
|
[NCBI]
|
0.00023161
|
|
|
anencephaly
|
[NCBI]
|
0.000230929
|
|
|
marden-walker syndrome
|
[NCBI]
|
0.000222553
|
|
|
CPI
|
[NCBI]
|
0.000211716
|
|
|
fraser syndrome
|
[NCBI]
|
0.000204252
|
|
|
por deficiency
|
[NCBI]
|
0.000200142
|
|
|
diaphragmatic hernia, congenital
|
[NCBI]
|
0.000181464
|
|
|
ACG2
|
[NCBI]
|
0.000181386
|
|
|
CF
|
[NCBI]
|
0.00017117
|
|
|
RTD
|
[NCBI]
|
0.000159933
|
|
|
PLSDT
|
[NCBI]
|
0.000137427
|
|
|
POR
|
[NCBI]
|
0.000128418
|
|
|
HAND1
|
[NCBI]
|
0.000125975
|
|
|
BOCD
|
[NCBI]
|
0.000118357
|
|
|
PEE1
|
[NCBI]
|
0.000117031
|
|
|
KLF1
|
[NCBI]
|
0.000116903
|
|
|
pseudotrisomy 13 syndrome
|
[NCBI]
|
0.000114963
|
|
|
antiphospholipid syndrome
|
[NCBI]
|
0.000111898
|
|
|
DWS
|
[NCBI]
|
0.000110828
|
|
|
AOS
|
[NCBI]
|
0.000110828
|
|
|
MKS1
|
[NCBI]
|
0.000107807
|
|
|
heterotopia, periventricular, x-linked dominant
|
[NCBI]
|
9.99001e-05
|
|
|
lethal short-limb skeletal dysplasia, al gazali type
|
[NCBI]
|
9.95569e-05
|
|
|
multiple congenital anomalies syndrome with cloverleaf skull
|
[NCBI]
|
9.95569e-05
|
|
|
fibuloulnar aplasia or hypoplasia with renal abnormalities
|
[NCBI]
|
9.95569e-05
|
|
|
osteogenesis imperfecta, sillence type ii/iii, without abnormality of type i collagen
|
[NCBI]
|
9.95569e-05
|
|
|
baby rattle pelvis dysplasia
|
[NCBI]
|
9.95569e-05
|
|
|
blood group--en
|
[NCBI]
|
9.95569e-05
|
|
|
TFAM
|
[NCBI]
|
9.84483e-05
|
|
|
F2RL3
|
[NCBI]
|
9.84483e-05
|
|
|
TD1
|
[NCBI]
|
9.47823e-05
|
|
|
NR6A1
|
[NCBI]
|
9.25763e-05
|
|
|
GSC
|
[NCBI]
|
8.80805e-05
|
|
|
PROCR
|
[NCBI]
|
8.69484e-05
|
|
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
8.2737e-05
|
|
|
SLOS
|
[NCBI]
|
8.17943e-05
|
|
|
FOLR1
|
[NCBI]
|
7.87067e-05
|
|
|
crane-heise syndrome
|
[NCBI]
|
7.7119e-05
|
|
|
craniomicromelic syndrome
|
[NCBI]
|
7.7119e-05
|
|
|
contractures, congenital, torticollis, and malignant hyperthermia
|
[NCBI]
|
7.7119e-05
|
|
|
thymic-renal-anal-lung dysplasia
|
[NCBI]
|
7.7119e-05
|
|
|
POMT1
|
[NCBI]
|
7.06867e-05
|
|
|
multiple pterygium syndrome, aslan type
|
[NCBI]
|
6.86717e-05
|
|
|
BDA6
|
[NCBI]
|
6.86717e-05
|
|
|
osteopetrosis and infantile neuroaxonal dystrophy
|
[NCBI]
|
6.86717e-05
|
|
|
pterygium syndrome, multiple, x-linked
|
[NCBI]
|
6.86717e-05
|
|
|
chylothorax, congenital
|
[NCBI]
|
6.31982e-05
|
|
|
DDSH
|
[NCBI]
|
6.31982e-05
|
|
|
aminopterin syndrome sine aminopterin
|
[NCBI]
|
6.31982e-05
|
|
|
PELO
|
[NCBI]
|
6.29681e-05
|
|
|
ESRRB
|
[NCBI]
|
6.29681e-05
|
|
|
FKBP1A
|
[NCBI]
|
6.29681e-05
|
|
|
IGKV1OR2108
|
[NCBI]
|
6.29681e-05
|
|
|
CCNB2
|
[NCBI]
|
6.29681e-05
|
|
|
MAP3K7IP2
|
[NCBI]
|
6.29681e-05
|
|
|
ROCK2
|
[NCBI]
|
6.29681e-05
|
|
|
MEP1B
|
[NCBI]
|
6.29681e-05
|
|
|
GCN5L2
|
[NCBI]
|
6.29681e-05
|
|
|
BWS
|
[NCBI]
|
6.18687e-05
|
|
|
pulmonary hypertension, familial persistent, of the newborn
|
[NCBI]
|
5.91371e-05
|
|
|
aprosencephaly syndrome
|
[NCBI]
|
5.91371e-05
|
|
|
malpuech facial clefting syndrome
|
[NCBI]
|
5.91371e-05
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
5.90629e-05
|
|
|
COL1A1
|
[NCBI]
|
5.67732e-05
|
|
|
isotretinoin embryopathy-like syndrome
|
[NCBI]
|
5.59078e-05
|
|
|
cleft lip/palate with abnormal thumbs and microcephaly
|
[NCBI]
|
5.59078e-05
|
|
|
weyers ulnar ray/oligodactyly syndrome
|
[NCBI]
|
5.59078e-05
|
|
|
IKBKG
|
[NCBI]
|
5.41032e-05
|
|
|
schneckenbecken dysplasia
|
[NCBI]
|
5.32282e-05
|
|
|
BMP4
|
[NCBI]
|
5.21315e-05
|
|
|
murcs association
|
[NCBI]
|
5.09393e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, lethal neonatal
|
[NCBI]
|
5.09393e-05
|
|
|
boomerang dysplasia
|
[NCBI]
|
5.09393e-05
|
|
|
oeis complex
|
[NCBI]
|
5.09393e-05
|
|
|
MTHFD2
|
[NCBI]
|
4.92049e-05
|
|
|
PLOD3
|
[NCBI]
|
4.92049e-05
|
|
|
STE
|
[NCBI]
|
4.92049e-05
|
|
|
TRRAP
|
[NCBI]
|
4.92049e-05
|
|
|
ADRA2A
|
[NCBI]
|
4.92049e-05
|
|
|
TNS1
|
[NCBI]
|
4.92049e-05
|
|
|
ATP5A1
|
[NCBI]
|
4.92049e-05
|
|
|
BIRC6
|
[NCBI]
|
4.92049e-05
|
|
|
TXN2
|
[NCBI]
|
4.92049e-05
|
|
|
TPST1
|
[NCBI]
|
4.92049e-05
|
|
|
MGAT1
|
[NCBI]
|
4.92049e-05
|
|
|
CUL1
|
[NCBI]
|
4.92049e-05
|
|
|
PRMT1
|
[NCBI]
|
4.92049e-05
|
|
|
ICMT
|
[NCBI]
|
4.92049e-05
|
|
|
ablepharon-macrostomia syndrome
|
[NCBI]
|
4.89425e-05
|
|
|
blood group, p system
|
[NCBI]
|
4.89425e-05
|
|
|
AVSD
|
[NCBI]
|
4.84752e-05
|
|
|
BPP
|
[NCBI]
|
4.71724e-05
|
|
|
MCOPS9
|
[NCBI]
|
4.55835e-05
|
|
|
MRXS13
|
[NCBI]
|
4.41426e-05
|
|
|
hydrolethalus syndrome 1
|
[NCBI]
|
4.41426e-05
|
|
|
AOI
|
[NCBI]
|
4.41426e-05
|
|
|
TEAD1
|
[NCBI]
|
4.40211e-05
|
|
|
ITGA6
|
[NCBI]
|
4.40211e-05
|
|
|
HTR2B
|
[NCBI]
|
4.40211e-05
|
|
|
IDH3G
|
[NCBI]
|
4.40211e-05
|
|
|
GRIP1
|
[NCBI]
|
4.40211e-05
|
|
|
NR2C2
|
[NCBI]
|
4.40211e-05
|
|
|
ACHE
|
[NCBI]
|
4.35345e-05
|
|
|
LQT3
|
[NCBI]
|
4.2825e-05
|
|
|
hydrocephalus
|
[NCBI]
|
4.2825e-05
|
|
|
vitamin k-dependent clotting factors, combined deficiency of, 1
|
[NCBI]
|
4.16116e-05
|
|
|
HPE2
|
[NCBI]
|
4.16116e-05
|
|
|
hemochromatosis, neonatal
|
[NCBI]
|
4.16116e-05
|
|
|
NR5A2
|
[NCBI]
|
4.06609e-05
|
|
|
CCNB1
|
[NCBI]
|
4.06609e-05
|
|
|
ATOX1
|
[NCBI]
|
4.06609e-05
|
|
|
DLAT
|
[NCBI]
|
4.06609e-05
|
|
|
LAMC1
|
[NCBI]
|
4.06609e-05
|
|
|
XRCC5
|
[NCBI]
|
4.06609e-05
|
|
|
EFEMP2
|
[NCBI]
|
4.06609e-05
|
|
|
MCL1
|
[NCBI]
|
4.06609e-05
|
|
|
GATA2
|
[NCBI]
|
4.06609e-05
|
|
|
rad54, s. cerevisiae, homolog of, b
|
[NCBI]
|
4.06609e-05
|
|
|
multiple pterygium syndrome, escobar variant
|
[NCBI]
|
4.04875e-05
|
|
|
caffey disease
|
[NCBI]
|
4.04875e-05
|
|
|
PTH
|
[NCBI]
|
3.97382e-05
|
|
|
chondrodysplasia punctata, autosomal dominant
|
[NCBI]
|
3.94409e-05
|
|
|
COFS1
|
[NCBI]
|
3.94409e-05
|
|
|
tetralogy of fallot
|
[NCBI]
|
3.94409e-05
|
|
|
CDLS1
|
[NCBI]
|
3.912e-05
|
|
|
afibrinogenemia, congenital
|
[NCBI]
|
3.84619e-05
|
|
|
MAPK9
|
[NCBI]
|
3.81668e-05
|
|
|
NCOA6
|
[NCBI]
|
3.81668e-05
|
|
|
A4GALT
|
[NCBI]
|
3.81668e-05
|
|
|
MST1R
|
[NCBI]
|
3.81668e-05
|
|
|
ITPR1
|
[NCBI]
|
3.81668e-05
|
|
|
MARCKS
|
[NCBI]
|
3.81668e-05
|
|
|
MTHFR
|
[NCBI]
|
3.77196e-05
|
|
|
papillorenal syndrome
|
[NCBI]
|
3.75426e-05
|
|
|
CDPX1
|
[NCBI]
|
3.66764e-05
|
|
|
CDX2
|
[NCBI]
|
3.61828e-05
|
|
|
FADD
|
[NCBI]
|
3.61828e-05
|
|
|
XBP1
|
[NCBI]
|
3.61828e-05
|
|
|
factor v deficiency
|
[NCBI]
|
3.50901e-05
|
|
|
IP
|
[NCBI]
|
3.46567e-05
|
|
|
FBXW7
|
[NCBI]
|
3.45358e-05
|
|
|
CITED2
|
[NCBI]
|
3.45358e-05
|
|
|
CCNA2
|
[NCBI]
|
3.45358e-05
|
|
|
ZIC2
|
[NCBI]
|
3.45358e-05
|
|
|
TFAP2A
|
[NCBI]
|
3.45358e-05
|
|
|
SCN2A
|
[NCBI]
|
3.45358e-05
|
|
|
BCAR1
|
[NCBI]
|
3.45358e-05
|
|
|
SFTPD
|
[NCBI]
|
3.45358e-05
|
|
|
LAMB1
|
[NCBI]
|
3.45358e-05
|
|
|
lymphedema-distichiasis syndrome
|
[NCBI]
|
3.43442e-05
|
|
|
MAP2K1
|
[NCBI]
|
3.31285e-05
|
|
|
JUN
|
[NCBI]
|
3.31285e-05
|
|
|
IGF2R
|
[NCBI]
|
3.31285e-05
|
|
|
PEG3
|
[NCBI]
|
3.31285e-05
|
|
|
BARD1
|
[NCBI]
|
3.31285e-05
|
|
|
DLL4
|
[NCBI]
|
3.31285e-05
|
|
|
TRAF2
|
[NCBI]
|
3.31285e-05
|
|
|
PAPPA
|
[NCBI]
|
3.31285e-05
|
|
|
MEST
|
[NCBI]
|
3.31285e-05
|
|
|
ECE1
|
[NCBI]
|
3.31285e-05
|
|
|
GBA
|
[NCBI]
|
3.3023e-05
|
|
|
HSS
|
[NCBI]
|
3.29717e-05
|
|
|
ADSL
|
[NCBI]
|
3.19003e-05
|
|
|
MAPK7
|
[NCBI]
|
3.19003e-05
|
|
|
PLCB3
|
[NCBI]
|
3.19003e-05
|
|
|
epidermolysis bullosa with pyloric atresia
|
[NCBI]
|
3.11284e-05
|
|
|
THBD
|
[NCBI]
|
3.08111e-05
|
|
|
RELA
|
[NCBI]
|
3.08111e-05
|
|
|
MT1A
|
[NCBI]
|
3.08111e-05
|
|
|
GSK3B
|
[NCBI]
|
3.08111e-05
|
|
|
central core disease of muscle
|
[NCBI]
|
3.00185e-05
|
|
|
FLI1
|
[NCBI]
|
2.9833e-05
|
|
|
SIRT1
|
[NCBI]
|
2.9833e-05
|
|
|
LIG4
|
[NCBI]
|
2.9833e-05
|
|
|
MST1
|
[NCBI]
|
2.9833e-05
|
|
|
CREB1
|
[NCBI]
|
2.9833e-05
|
|
|
EGF
|
[NCBI]
|
2.97395e-05
|
|
|
OKS
|
[NCBI]
|
2.94942e-05
|
|
|
ABS
|
[NCBI]
|
2.94942e-05
|
|
|
MKKS
|
[NCBI]
|
2.89886e-05
|
|
|
MAPK8
|
[NCBI]
|
2.89456e-05
|
|
|
GATA3
|
[NCBI]
|
2.89456e-05
|
|
|
LDHA
|
[NCBI]
|
2.89456e-05
|
|
|
TSG101
|
[NCBI]
|
2.89456e-05
|
|
|
HSAS
|
[NCBI]
|
2.85004e-05
|
|
|
E2F1
|
[NCBI]
|
2.81339e-05
|
|
|
CPT2
|
[NCBI]
|
2.81339e-05
|
|
|
pfeiffer syndrome
|
[NCBI]
|
2.80286e-05
|
|
|
SGBS1
|
[NCBI]
|
2.75721e-05
|
|
|
DGS
|
[NCBI]
|
2.69511e-05
|
|
|
CBFA2T1
|
[NCBI]
|
2.66931e-05
|
|
|
hypophosphatasia, infantile
|
[NCBI]
|
2.62862e-05
|
|
|
TBS
|
[NCBI]
|
2.62862e-05
|
|
|
CDPX2
|
[NCBI]
|
2.62862e-05
|
|
|
SEDC
|
[NCBI]
|
2.62862e-05
|
|
|
apert syndrome
|
[NCBI]
|
2.62862e-05
|
|
|
GK
|
[NCBI]
|
2.60475e-05
|
|
|
CASP8
|
[NCBI]
|
2.60475e-05
|
|
|
MEB
|
[NCBI]
|
2.58829e-05
|
|
|
LIFR
|
[NCBI]
|
2.54434e-05
|
|
|
CXCR4
|
[NCBI]
|
2.54434e-05
|
|
|
TPT1
|
[NCBI]
|
2.54434e-05
|
|
|
walker-warburg syndrome
|
[NCBI]
|
2.47398e-05
|
|
|
MAP1B
|
[NCBI]
|
2.4341e-05
|
|
|
FOXC2
|
[NCBI]
|
2.4341e-05
|
|
|
KLF6
|
[NCBI]
|
2.4341e-05
|
|
|
TRPS2
|
[NCBI]
|
2.4028e-05
|
|
|
campomelic dysplasia
|
[NCBI]
|
2.4028e-05
|
|
|
DKC1
|
[NCBI]
|
2.38352e-05
|
|
|
3-@hydroxy-3-methylglutaryl-coa lyase deficiency
|
[NCBI]
|
2.33556e-05
|
|
|
DHCR7
|
[NCBI]
|
2.33556e-05
|
|
|
NOTCH1
|
[NCBI]
|
2.33556e-05
|
|
|
FDH
|
[NCBI]
|
2.33522e-05
|
|
|
SPTB
|
[NCBI]
|
2.28996e-05
|
|
|
ATR
|
[NCBI]
|
2.28996e-05
|
|
|
PRL
|
[NCBI]
|
2.26036e-05
|
|
|
EDN1
|
[NCBI]
|
2.24653e-05
|
|
|
PAX2
|
[NCBI]
|
2.24653e-05
|
|
|
H19
|
[NCBI]
|
2.24653e-05
|
|
|
SOCS1
|
[NCBI]
|
2.24653e-05
|
|
|
FGG
|
[NCBI]
|
2.24653e-05
|
|
|
ADM
|
[NCBI]
|
2.19795e-05
|
|
|
ALPL
|
[NCBI]
|
2.12737e-05
|
|
|
CHM
|
[NCBI]
|
2.06799e-05
|
|
|
NBS1
|
[NCBI]
|
2.05583e-05
|
|
|
FCMD
|
[NCBI]
|
1.99e-05
|
|
|
TNF
|
[NCBI]
|
1.98713e-05
|
|
|
SOCS3
|
[NCBI]
|
1.92787e-05
|
|
|
F3
|
[NCBI]
|
1.90784e-05
|
|
|
HOS
|
[NCBI]
|
1.89305e-05
|
|
|
MFS
|
[NCBI]
|
1.87818e-05
|
|
|
MG
|
[NCBI]
|
1.87423e-05
|
|
|
RECQL2
|
[NCBI]
|
1.8702e-05
|
|
|
PDHA1
|
[NCBI]
|
1.8702e-05
|
|
|
ASPA
|
[NCBI]
|
1.79022e-05
|
|
|
FLNA
|
[NCBI]
|
1.79022e-05
|
|
|
ENG
|
[NCBI]
|
1.76511e-05
|
|
|
F2R
|
[NCBI]
|
1.74071e-05
|
|
|
coproporphyria
|
[NCBI]
|
1.74071e-05
|
|
|
AMC
|
[NCBI]
|
1.71961e-05
|
|
|
ATRX
|
[NCBI]
|
1.71698e-05
|
|
|
RUNX1
|
[NCBI]
|
1.71698e-05
|
|
|
MTATP6
|
[NCBI]
|
1.71698e-05
|
|
|
A2M
|
[NCBI]
|
1.6495e-05
|
|
|
factor x deficiency
|
[NCBI]
|
1.62814e-05
|
|
|
F2
|
[NCBI]
|
1.54774e-05
|
|
|
NOS3
|
[NCBI]
|
1.51026e-05
|
|
|
factor vii deficiency
|
[NCBI]
|
1.51026e-05
|
|
|
SCN5A
|
[NCBI]
|
1.47441e-05
|
|
|
FXN
|
[NCBI]
|
1.47441e-05
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
1.43509e-05
|
|
|
PKD2
|
[NCBI]
|
1.4071e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
1.40641e-05
|
|
|
menkes disease
|
[NCBI]
|
1.40414e-05
|
|
|
glycogen storage disease i
|
[NCBI]
|
1.36006e-05
|
|
|
thrombasthenia of glanzmann and naegeli
|
[NCBI]
|
1.35933e-05
|
|
|
MAP3K5
|
[NCBI]
|
1.34497e-05
|
|
|
LS
|
[NCBI]
|
1.31634e-05
|
|
|
RYR1
|
[NCBI]
|
1.26004e-05
|
|
|
LBP
|
[NCBI]
|
1.26004e-05
|
|
|
CPB2
|
[NCBI]
|
1.24674e-05
|
|
|
cortisol 11-beta-ketoreductase deficiency
|
[NCBI]
|
1.22081e-05
|
|
|
TSC2
|
[NCBI]
|
1.20816e-05
|
|
|
SRF
|
[NCBI]
|
1.14792e-05
|
|
|
COL2A1
|
[NCBI]
|
1.12511e-05
|
|
|
VHL
|
[NCBI]
|
1.11396e-05
|
|
|
SHH
|
[NCBI]
|
1.04463e-05
|
|
|
FRDA
|
[NCBI]
|
1.02607e-05
|
|
|
EPOR
|
[NCBI]
|
1.00141e-05
|
|
|
PCNA
|
[NCBI]
|
9.93869e-06
|
|
|
NPM1
|
[NCBI]
|
9.64519e-06
|
|
|
JAK2
|
[NCBI]
|
9.3808e-06
|
|
|
ABCG2
|
[NCBI]
|
9.12622e-06
|
|
|
DNMT1
|
[NCBI]
|
8.49101e-06
|
|
|
MBP
|
[NCBI]
|
7.79988e-06
|
|
|
MEN1
|
[NCBI]
|
7.51013e-06
|
|
|
BRCA2
|
[NCBI]
|
7.31858e-06
|
|
|
CMH
|
[NCBI]
|
7.22307e-06
|
|
|
MECP2
|
[NCBI]
|
7.01222e-06
|
|
|
FGFR2
|
[NCBI]
|
6.66438e-06
|
|
|
apc gene
|
[NCBI]
|
5.82923e-06
|
|
|
VEGF
|
[NCBI]
|
5.6045e-06
|
|
|
TSD
|
[NCBI]
|
4.77115e-06
|
|
|
GPI
|
[NCBI]
|
4.74255e-06
|
|
|
TH
|
[NCBI]
|
4.55396e-06
|
|
|
WBS
|
[NCBI]
|
4.48303e-06
|
|
|
EPO
|
[NCBI]
|
4.30105e-06
|
|
|
TS
|
[NCBI]
|
4.25806e-06
|
|
|
PPARA
|
[NCBI]
|
3.93129e-06
|
|
|
BRCA1
|
[NCBI]
|
3.76503e-06
|
|
|
phenylketonuria
|
[NCBI]
|
3.1593e-06
|
|
|
RB1
|
[NCBI]
|
3.05433e-06
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
3.03812e-06
|
|
|
VIP
|
[NCBI]
|
1.64987e-06
|
|
|
AHR
|
[NCBI]
|
1.55655e-06
|
|
|
GNRH1
|
[NCBI]
|
1.07796e-06
|
|
|
GFAP
|
[NCBI]
|
1.05107e-06
|
|
|
HGF
|
[NCBI]
|
1.04145e-06
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
7.99603e-07
|
|
|
ADA
|
[NCBI]
|
7.648e-07
|
|
|
TFPI
|
[NCBI]
|
5.12862e-07
|
|
|
MUC1
|
[NCBI]
|
4.47724e-07
|
|
|
G6PD
|
[NCBI]
|
1.3393e-07
|
|
|
HD
|
[NCBI]
|
1.21953e-07
|
|
|
DHFR
|
[NCBI]
|
6.89655e-08
|
|
|
TG
|
[NCBI]
|
5.06297e-08
|
|
|
APOB
|
[NCBI]
|
9.69218e-11
|
|