|
OMIM |
Link |
Information gain |
01 |
|
robinow syndrome, autosomal dominant
|
[NCBI]
|
0.00490173
|
|
|
faciodigitogenital syndrome, recessive
|
[NCBI]
|
0.00425954
|
|
|
faciogenital dysplasia
|
[NCBI]
|
0.00144698
|
|
|
umbilicus, familial flat
|
[NCBI]
|
0.0014006
|
|
|
AIS
|
[NCBI]
|
0.00121625
|
|
|
deafness, conductive, with malformed external ear
|
[NCBI]
|
0.00109002
|
|
|
peyronie disease
|
[NCBI]
|
0.00109002
|
|
|
AR
|
[NCBI]
|
0.00103833
|
|
|
SHFM5
|
[NCBI]
|
0.00097306
|
|
|
MCOPS6
|
[NCBI]
|
0.000796235
|
|
|
OD
|
[NCBI]
|
0.000496828
|
|
|
PPSH
|
[NCBI]
|
0.000327131
|
|
|
myotubular myopathy with abnormal genital development
|
[NCBI]
|
0.000305103
|
|
|
aarskog syndrome
|
[NCBI]
|
0.000305103
|
|
|
intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies
|
[NCBI]
|
0.0002807
|
|
|
LISX2
|
[NCBI]
|
0.000263963
|
|
|
disorganization, mouse, homolog of
|
[NCBI]
|
0.000231993
|
|
|
leopard syndrome 1
|
[NCBI]
|
0.000211832
|
|
|
denys-drash syndrome
|
[NCBI]
|
0.000211832
|
|
|
cardiogenital syndrome
|
[NCBI]
|
0.000179421
|
|
|
scarf syndrome
|
[NCBI]
|
0.000179421
|
|
|
hypomelia with mullerian duct anomalies
|
[NCBI]
|
0.000179421
|
|
|
macdermot-winter syndrome
|
[NCBI]
|
0.000179421
|
|
|
pelviscapular dysplasia
|
[NCBI]
|
0.000179421
|
|
|
beemer lethal malformation syndrome
|
[NCBI]
|
0.000179421
|
|
|
faciothoracogenital syndrome
|
[NCBI]
|
0.000179421
|
|
|
hemolytic anemia, lethal congenital nonspherocytic, with genital and other abnormalities
|
[NCBI]
|
0.000179421
|
|
|
PFM
|
[NCBI]
|
0.000167674
|
|
|
charge syndrome
|
[NCBI]
|
0.000162839
|
|
|
OKS
|
[NCBI]
|
0.000162839
|
|
|
cree mental retardation syndrome
|
[NCBI]
|
0.000140193
|
|
|
hypogonadism, male
|
[NCBI]
|
0.000140193
|
|
|
hypospadias, x-linked
|
[NCBI]
|
0.000140193
|
|
|
prader-willi habitus, osteopenia, and camptodactyly
|
[NCBI]
|
0.000140193
|
|
|
SERKAL
|
[NCBI]
|
0.000140193
|
|
|
corpus callosum, agenesis of, with abnormal genitalia
|
[NCBI]
|
0.000140193
|
|
|
cleft palate, cardiac defect, genital anomalies, and ectrodactyly
|
[NCBI]
|
0.000140193
|
|
|
NS1
|
[NCBI]
|
0.000127053
|
|
|
MKS1
|
[NCBI]
|
0.000125884
|
|
|
AMH
|
[NCBI]
|
0.000125361
|
|
|
camptomelic syndrome, long-limb type
|
[NCBI]
|
0.000115841
|
|
|
laurence-moon syndrome
|
[NCBI]
|
0.000115841
|
|
|
pelvis-shoulder dysplasia
|
[NCBI]
|
0.000115841
|
|
|
WT1
|
[NCBI]
|
0.000106423
|
|
|
vacterl association with hydrocephalus, x-linked
|
[NCBI]
|
0.000103078
|
|
|
ruvalcaba syndrome
|
[NCBI]
|
0.000103078
|
|
|
young syndrome
|
[NCBI]
|
0.000103078
|
|
|
BBS
|
[NCBI]
|
9.73794e-05
|
|
|
ablepharon-macrostomia syndrome
|
[NCBI]
|
9.43724e-05
|
|
|
GNRH1
|
[NCBI]
|
8.97347e-05
|
|
|
vater association
|
[NCBI]
|
8.77672e-05
|
|
|
hand-foot-uterus syndrome
|
[NCBI]
|
8.49794e-05
|
|
|
wagr syndrome
|
[NCBI]
|
8.49794e-05
|
|
|
MCOPS3
|
[NCBI]
|
8.24503e-05
|
|
|
lipoid congenital adrenal hyperplasia
|
[NCBI]
|
8.24503e-05
|
|
|
seckel syndrome 1
|
[NCBI]
|
8.24503e-05
|
|
|
SLOS
|
[NCBI]
|
7.81117e-05
|
|
|
PMDS
|
[NCBI]
|
7.80052e-05
|
|
|
PRL
|
[NCBI]
|
7.32053e-05
|
|
|
growth hormone insensitivity syndrome
|
[NCBI]
|
7.08505e-05
|
|
|
UMS
|
[NCBI]
|
6.7884e-05
|
|
|
CBAVD
|
[NCBI]
|
6.7884e-05
|
|
|
robinow syndrome, autosomal recessive
|
[NCBI]
|
6.65169e-05
|
|
|
MRXHF1
|
[NCBI]
|
6.39793e-05
|
|
|
ATRX
|
[NCBI]
|
6.27972e-05
|
|
|
SHBG
|
[NCBI]
|
5.88324e-05
|
|
|
ARX
|
[NCBI]
|
5.34655e-05
|
|
|
MDLS
|
[NCBI]
|
5.09727e-05
|
|
|
NR0B1
|
[NCBI]
|
4.57914e-05
|
|
|
KLK3
|
[NCBI]
|
4.36745e-05
|
|
|
NPY
|
[NCBI]
|
4.27741e-05
|
|
|
SLC18A3
|
[NCBI]
|
4.18194e-05
|
|
|
MTM1
|
[NCBI]
|
4.09916e-05
|
|
|
SEMG
|
[NCBI]
|
4.08055e-05
|
|
|
ARID5B
|
[NCBI]
|
3.70435e-05
|
|
|
SRY
|
[NCBI]
|
3.47359e-05
|
|
|
CXORF6
|
[NCBI]
|
3.46026e-05
|
|
|
WT1
|
[NCBI]
|
3.16959e-05
|
|
|
SRD5A2
|
[NCBI]
|
3.13453e-05
|
|
|
SEMA3E
|
[NCBI]
|
3.13453e-05
|
|
|
SRD5A1
|
[NCBI]
|
3.13453e-05
|
|
|
SIX6
|
[NCBI]
|
3.13453e-05
|
|
|
FANCB
|
[NCBI]
|
3.01456e-05
|
|
|
PODXL
|
[NCBI]
|
2.91195e-05
|
|
|
WNT4
|
[NCBI]
|
2.82231e-05
|
|
|
SMAX1
|
[NCBI]
|
2.39314e-05
|
|
|
PTGS1
|
[NCBI]
|
2.3493e-05
|
|
|
SOX2
|
[NCBI]
|
2.30753e-05
|
|
|
FGF9
|
[NCBI]
|
2.30753e-05
|
|
|
DCX
|
[NCBI]
|
2.16174e-05
|
|
|
TFPI2
|
[NCBI]
|
1.96309e-05
|
|
|
FOLH1
|
[NCBI]
|
1.91548e-05
|
|
|
ESR2
|
[NCBI]
|
1.89287e-05
|
|
|
ATRX
|
[NCBI]
|
1.84978e-05
|
|
|
LHCGR
|
[NCBI]
|
1.684e-05
|
|
|
APOD
|
[NCBI]
|
1.60701e-05
|
|
|
ENPEP
|
[NCBI]
|
1.48765e-05
|
|
|
ESR1
|
[NCBI]
|
1.4187e-05
|
|
|
EGF
|
[NCBI]
|
1.2241e-05
|
|
|
PTGS2
|
[NCBI]
|
1.20734e-05
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
1.19959e-05
|
|
|
PIGR
|
[NCBI]
|
1.10027e-05
|
|
|
FGFR1
|
[NCBI]
|
1.03818e-05
|
|
|
BWS
|
[NCBI]
|
1.03264e-05
|
|
|
RBP1
|
[NCBI]
|
9.71405e-06
|
|
|
SERPINA6
|
[NCBI]
|
7.668e-06
|
|
|
ABP1
|
[NCBI]
|
7.05325e-06
|
|
|
ACHE
|
[NCBI]
|
6.82736e-06
|
|
|
ACE
|
[NCBI]
|
6.5052e-06
|
|
|
AKR1B1
|
[NCBI]
|
5.56691e-06
|
|
|
CFTR
|
[NCBI]
|
5.55117e-06
|
|
|
CAT
|
[NCBI]
|
4.67827e-06
|
|
|
HDC
|
[NCBI]
|
4.59786e-06
|
|
|
STAR
|
[NCBI]
|
3.94064e-06
|
|
|
CHAT
|
[NCBI]
|
1.8074e-06
|
|
|
TF
|
[NCBI]
|
1.35832e-06
|
|
|
NGFB
|
[NCBI]
|
1.02531e-06
|
|
|
PWS
|
[NCBI]
|
9.58892e-07
|
|
|
ADCYAP1
|
[NCBI]
|
8.26777e-07
|
|
|
CRH
|
[NCBI]
|
5.70185e-07
|
|
|
POMC
|
[NCBI]
|
5.43113e-07
|
|
|
AHR
|
[NCBI]
|
4.54738e-07
|
|
|
EGFR
|
[NCBI]
|
3.6578e-07
|
|
|
SPP1
|
[NCBI]
|
2.76046e-07
|
|
|
CF
|
[NCBI]
|
2.15339e-07
|
|
|
SHH
|
[NCBI]
|
1.97444e-07
|
|
|
TH
|
[NCBI]
|
1.4333e-07
|
|
|
PCNA
|
[NCBI]
|
1.33342e-07
|
|
|
VIP
|
[NCBI]
|
1.19603e-07
|
|