|
OMIM |
Link |
Information gain |
01 |
|
CES
|
[NCBI]
|
0.00140297
|
|
|
TBS
|
[NCBI]
|
0.00129976
|
|
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
0.000930625
|
|
|
cdags syndrome
|
[NCBI]
|
0.000900049
|
|
|
anorectal anomalies
|
[NCBI]
|
0.000900049
|
|
|
HFM
|
[NCBI]
|
0.000795904
|
|
|
exstrophy of bladder
|
[NCBI]
|
0.000724991
|
|
|
oeis complex
|
[NCBI]
|
0.000603463
|
|
|
PHS
|
[NCBI]
|
0.000565705
|
|
|
ACC
|
[NCBI]
|
0.000521852
|
|
|
OKS
|
[NCBI]
|
0.000433364
|
|
|
vater association
|
[NCBI]
|
0.000333365
|
|
|
SALL1
|
[NCBI]
|
0.000294842
|
|
|
JBS
|
[NCBI]
|
0.000275154
|
|
|
anus, imperforate
|
[NCBI]
|
0.000224694
|
|
|
anus, imperforate
|
[NCBI]
|
0.000224694
|
|
|
spondylocostal dysostosis with anal atresia and urogenital anomalies
|
[NCBI]
|
0.000193755
|
|
|
anal atresia, hypospadias, and penoscrotal inversion
|
[NCBI]
|
0.00017978
|
|
|
cleft larynx, posterior
|
[NCBI]
|
0.000162847
|
|
|
vacterl association with hydrocephalus, x-linked
|
[NCBI]
|
0.000147522
|
|
|
FANCB
|
[NCBI]
|
0.000142221
|
|
|
GLI3
|
[NCBI]
|
0.000115434
|
|
|
hair whorl
|
[NCBI]
|
0.000112254
|
|
|
aphalangy with hemivertebrae
|
[NCBI]
|
0.000112254
|
|
|
growth and developmental retardation, ocular ptosis, cardiac defect, and anal atresia
|
[NCBI]
|
0.000112254
|
|
|
polydactyly, imperforate anus, and vertebral anomalies
|
[NCBI]
|
0.000112254
|
|
|
cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction
|
[NCBI]
|
0.000112254
|
|
|
GCPS
|
[NCBI]
|
9.27342e-05
|
|
|
CECR1
|
[NCBI]
|
9.15682e-05
|
|
|
dk phocomelia syndrome
|
[NCBI]
|
8.97971e-05
|
|
|
stratton-parker syndrome
|
[NCBI]
|
8.97971e-05
|
|
|
thymic-renal-anal-lung dysplasia
|
[NCBI]
|
8.97971e-05
|
|
|
omphalocele, diaphragmatic hernia, and radial ray defects
|
[NCBI]
|
8.13307e-05
|
|
|
ivic syndrome
|
[NCBI]
|
7.58383e-05
|
|
|
GLI2
|
[NCBI]
|
6.9211e-05
|
|
|
SMOH
|
[NCBI]
|
6.9211e-05
|
|
|
vacterl association with hydrocephalus
|
[NCBI]
|
6.35035e-05
|
|
|
tracheoesophageal fistula with or without esophageal atresia
|
[NCBI]
|
6.35035e-05
|
|
|
polydactyly, postaxial, type a1
|
[NCBI]
|
6.35035e-05
|
|
|
T
|
[NCBI]
|
6.3036e-05
|
|
|
GLI
|
[NCBI]
|
6.3036e-05
|
|
|
currarino syndrome
|
[NCBI]
|
5.40619e-05
|
|
|
feingold syndrome
|
[NCBI]
|
5.29189e-05
|
|
|
PTCH1
|
[NCBI]
|
5.11499e-05
|
|
|
waardenburg-shah syndrome
|
[NCBI]
|
4.9917e-05
|
|
|
NR5A1
|
[NCBI]
|
4.94573e-05
|
|
|
UMS
|
[NCBI]
|
4.81941e-05
|
|
|
ABS
|
[NCBI]
|
4.16409e-05
|
|
|
MKKS
|
[NCBI]
|
4.11163e-05
|
|
|
fraser syndrome
|
[NCBI]
|
4.06092e-05
|
|
|
MTTL1
|
[NCBI]
|
3.80819e-05
|
|
|
charge syndrome
|
[NCBI]
|
3.78777e-05
|
|
|
CMTC
|
[NCBI]
|
3.48698e-05
|
|
|
hypogonadotropic hypogonadism
|
[NCBI]
|
2.56305e-05
|
|
|
SHH
|
[NCBI]
|
2.43406e-05
|
|
|
ACHE
|
[NCBI]
|
1.16939e-05
|
|
|
AFP
|
[NCBI]
|
6.79479e-06
|
|
|
FA
|
[NCBI]
|
2.15492e-06
|
|