|
OMIM |
Link |
Information gain |
01 |
|
OFC1
|
[NCBI]
|
0.0346564
|
|
|
CPI
|
[NCBI]
|
0.00973138
|
|
|
EEC1
|
[NCBI]
|
0.00759279
|
|
|
VWS
|
[NCBI]
|
0.00419869
|
|
|
OFC3
|
[NCBI]
|
0.00330786
|
|
|
blepharocheilodontic syndrome
|
[NCBI]
|
0.00327015
|
|
|
hypertelorism, microtia, facial clefting syndrome
|
[NCBI]
|
0.00264401
|
|
|
orofacial cleft 4
|
[NCBI]
|
0.00198131
|
|
|
OFC2
|
[NCBI]
|
0.00198131
|
|
|
rosselli-gulienetti syndrome
|
[NCBI]
|
0.00163
|
|
|
PPS
|
[NCBI]
|
0.00139246
|
|
|
acromelic frontonasal dysostosis
|
[NCBI]
|
0.00133447
|
|
|
short rib-polydactyly syndrome, type ii
|
[NCBI]
|
0.00125739
|
|
|
OFD5
|
[NCBI]
|
0.00102188
|
|
|
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging
|
[NCBI]
|
0.000863483
|
|
|
IRF6
|
[NCBI]
|
0.000823296
|
|
|
holoprosencephaly
|
[NCBI]
|
0.000777815
|
|
|
palatopharyngeal incompetence
|
[NCBI]
|
0.000713014
|
|
|
van der woude syndrome 2
|
[NCBI]
|
0.00065931
|
|
|
orofacial cleft 9
|
[NCBI]
|
0.00065931
|
|
|
short stature, mental retardation, callosal agenesis, heminasal hypoplasia, microphthalmia, and atypical clefting
|
[NCBI]
|
0.00065931
|
|
|
popliteal pterygium syndrome, lethal type
|
[NCBI]
|
0.000626637
|
|
|
THAS
|
[NCBI]
|
0.000551919
|
|
|
cleft, median, of upper lip with polyps of facial skin and nasal mucosa
|
[NCBI]
|
0.000542367
|
|
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
0.000539048
|
|
|
ankyloblepharon-ectodermal defects-cleft lip/palate
|
[NCBI]
|
0.000516289
|
|
|
CLPED1
|
[NCBI]
|
0.000516289
|
|
|
RBS
|
[NCBI]
|
0.000478745
|
|
|
constricting bands, congenital
|
[NCBI]
|
0.000445423
|
|
|
varadi-papp syndrome
|
[NCBI]
|
0.000424445
|
|
|
RHS
|
[NCBI]
|
0.000417097
|
|
|
van der woude syndrome modifier
|
[NCBI]
|
0.000363849
|
|
|
DA4
|
[NCBI]
|
0.000363849
|
|
|
frontofacionasal dysostosis
|
[NCBI]
|
0.000363849
|
|
|
immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum
|
[NCBI]
|
0.000363849
|
|
|
orofacial cleft 5
|
[NCBI]
|
0.000361386
|
|
|
PHF8
|
[NCBI]
|
0.00030601
|
|
|
EEC3
|
[NCBI]
|
0.00028564
|
|
|
MSX1
|
[NCBI]
|
0.000280571
|
|
|
microcephaly, corpus callosum dysgenesis, and cleft lip/palate
|
[NCBI]
|
0.000270968
|
|
|
coloboma, uveal, with cleft lip and palate and mental retardation
|
[NCBI]
|
0.000270968
|
|
|
siderius x-linked mental retardation syndrome
|
[NCBI]
|
0.000270968
|
|
|
TP73L
|
[NCBI]
|
0.000258622
|
|
|
AIC
|
[NCBI]
|
0.000258045
|
|
|
fryns microphthalmia syndrome
|
[NCBI]
|
0.000234566
|
|
|
HPE2
|
[NCBI]
|
0.000226223
|
|
|
short rib-polydactyly syndrome, type i
|
[NCBI]
|
0.000222248
|
|
|
LMS
|
[NCBI]
|
0.000221049
|
|
|
pallister w syndrome
|
[NCBI]
|
0.000180597
|
|
|
tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities
|
[NCBI]
|
0.000180597
|
|
|
cleft lip/palate with characteristic facies, intestinal malrotation, and lethal congenital heart disease
|
[NCBI]
|
0.000180597
|
|
|
holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate
|
[NCBI]
|
0.000180597
|
|
|
orofacial cleft 6
|
[NCBI]
|
0.000180597
|
|
|
cleft palate, cardiac defect, genital anomalies, and ectrodactyly
|
[NCBI]
|
0.000180597
|
|
|
KAL2
|
[NCBI]
|
0.000179194
|
|
|
PVRL1
|
[NCBI]
|
0.00017236
|
|
|
gordon syndrome
|
[NCBI]
|
0.000169655
|
|
|
DA5
|
[NCBI]
|
0.000169655
|
|
|
oculocerebrocutaneous syndrome
|
[NCBI]
|
0.000162132
|
|
|
adult syndrome
|
[NCBI]
|
0.000157741
|
|
|
OFD4
|
[NCBI]
|
0.000156291
|
|
|
short rib-polydactyly syndrome, type iii
|
[NCBI]
|
0.000156291
|
|
|
MTHFR
|
[NCBI]
|
0.000155667
|
|
|
TBX10
|
[NCBI]
|
0.000152704
|
|
|
HFM
|
[NCBI]
|
0.000151488
|
|
|
ankyloblepharon filiforme adnatum and cleft palate
|
[NCBI]
|
0.000149704
|
|
|
sakoda complex
|
[NCBI]
|
0.000149704
|
|
|
POADS
|
[NCBI]
|
0.000133632
|
|
|
holzgreve syndrome
|
[NCBI]
|
0.000126233
|
|
|
malpuech facial clefting syndrome
|
[NCBI]
|
0.000126233
|
|
|
mohr syndrome
|
[NCBI]
|
0.000123912
|
|
|
cleft lip/palate with abnormal thumbs and microcephaly
|
[NCBI]
|
0.000118934
|
|
|
OFD1
|
[NCBI]
|
0.000117954
|
|
|
frontonasal dysplasia
|
[NCBI]
|
0.000108041
|
|
|
SLC19A1
|
[NCBI]
|
0.000108011
|
|
|
GABRB3
|
[NCBI]
|
9.90021e-05
|
|
|
tibia, absence or hypoplasia of, with polydactyly, retrocerebellar arachnoid cyst, and other anomalies
|
[NCBI]
|
9.02749e-05
|
|
|
arthrogryposis, ectodermal dysplasia, cleft lip/palate, and developmental delay
|
[NCBI]
|
9.02749e-05
|
|
|
sao paulo mca/mr syndrome
|
[NCBI]
|
9.02749e-05
|
|
|
midline malformations, multiple, with limb abnormalities and hypopituitarism
|
[NCBI]
|
9.02749e-05
|
|
|
radius, aplasia of, with cleft lip/palate
|
[NCBI]
|
9.02749e-05
|
|
|
cerebrorenodigital syndrome with limb malformations and triradiate acetabula
|
[NCBI]
|
9.02749e-05
|
|
|
cleft lip, congenital healed
|
[NCBI]
|
9.02749e-05
|
|
|
cardiac malformation, cleft lip-palate, microcephaly and digital anomalies
|
[NCBI]
|
9.02749e-05
|
|
|
reese retinal dysplasia
|
[NCBI]
|
9.02749e-05
|
|
|
DA2B
|
[NCBI]
|
8.82624e-05
|
|
|
robinow syndrome, autosomal dominant
|
[NCBI]
|
8.62909e-05
|
|
|
SMMCI
|
[NCBI]
|
7.8005e-05
|
|
|
FGF8
|
[NCBI]
|
7.72352e-05
|
|
|
SCD5
|
[NCBI]
|
7.62777e-05
|
|
|
CLPTM1
|
[NCBI]
|
7.62777e-05
|
|
|
arthrogryposis, distal, type 2e
|
[NCBI]
|
6.78641e-05
|
|
|
crane-heise syndrome
|
[NCBI]
|
6.78641e-05
|
|
|
telecanthus
|
[NCBI]
|
6.78641e-05
|
|
|
OFD7
|
[NCBI]
|
6.78641e-05
|
|
|
acrofrontofacionasal dysostosis syndrome
|
[NCBI]
|
6.78641e-05
|
|
|
OSR2
|
[NCBI]
|
6.25015e-05
|
|
|
LHX8
|
[NCBI]
|
6.25015e-05
|
|
|
twirler mutation, murine, human homolog of
|
[NCBI]
|
6.25015e-05
|
|
|
chands
|
[NCBI]
|
5.94438e-05
|
|
|
KPC
|
[NCBI]
|
5.94438e-05
|
|
|
lowry-maclean syndrome
|
[NCBI]
|
5.94438e-05
|
|
|
albinism, ocular, with sensorineural deafness
|
[NCBI]
|
5.94438e-05
|
|
|
brachial amelia, forebrain defects, and facial clefts
|
[NCBI]
|
5.94438e-05
|
|
|
carnevale syndrome
|
[NCBI]
|
5.94438e-05
|
|
|
FGFR1
|
[NCBI]
|
5.86572e-05
|
|
|
ARNT2
|
[NCBI]
|
5.73046e-05
|
|
|
SNX3
|
[NCBI]
|
5.73046e-05
|
|
|
aminopterin syndrome sine aminopterin
|
[NCBI]
|
5.39973e-05
|
|
|
MCOPS8
|
[NCBI]
|
5.39973e-05
|
|
|
tetra-amelia, autosomal recessive
|
[NCBI]
|
5.39973e-05
|
|
|
oculopalatoskeletal syndrome
|
[NCBI]
|
5.39973e-05
|
|
|
PDGFC
|
[NCBI]
|
5.39314e-05
|
|
|
walker-warburg syndrome
|
[NCBI]
|
5.34605e-05
|
|
|
NLS
|
[NCBI]
|
5.2546e-05
|
|
|
ESCO2
|
[NCBI]
|
5.14243e-05
|
|
|
SUMO1
|
[NCBI]
|
5.14243e-05
|
|
|
keratitis, hereditary
|
[NCBI]
|
4.99632e-05
|
|
|
ICSBP1
|
[NCBI]
|
4.94272e-05
|
|
|
STHAG1
|
[NCBI]
|
4.6761e-05
|
|
|
fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly
|
[NCBI]
|
4.6761e-05
|
|
|
tibial hemimelia
|
[NCBI]
|
4.6761e-05
|
|
|
cleft larynx, posterior
|
[NCBI]
|
4.6761e-05
|
|
|
SHFM4
|
[NCBI]
|
4.6761e-05
|
|
|
MID1
|
[NCBI]
|
4.63469e-05
|
|
|
FOLR1
|
[NCBI]
|
4.51057e-05
|
|
|
EFNB1
|
[NCBI]
|
4.51057e-05
|
|
|
BHMT
|
[NCBI]
|
4.30123e-05
|
|
|
MKS1
|
[NCBI]
|
4.20306e-05
|
|
|
WS1
|
[NCBI]
|
4.15474e-05
|
|
|
HSD11B1
|
[NCBI]
|
4.05263e-05
|
|
|
peters-plus syndrome
|
[NCBI]
|
3.98768e-05
|
|
|
FGFR3
|
[NCBI]
|
3.96872e-05
|
|
|
KNO
|
[NCBI]
|
3.81338e-05
|
|
|
trismus-pseudocamptodactyly syndrome
|
[NCBI]
|
3.81338e-05
|
|
|
opitz syndrome
|
[NCBI]
|
3.81338e-05
|
|
|
DA1
|
[NCBI]
|
3.65719e-05
|
|
|
pseudotrisomy 13 syndrome
|
[NCBI]
|
3.65719e-05
|
|
|
EYA1
|
[NCBI]
|
3.64046e-05
|
|
|
EDN1
|
[NCBI]
|
3.54882e-05
|
|
|
hydrolethalus syndrome 1
|
[NCBI]
|
3.5158e-05
|
|
|
RARA
|
[NCBI]
|
3.50605e-05
|
|
|
AHR
|
[NCBI]
|
3.43729e-05
|
|
|
LADD
|
[NCBI]
|
3.38675e-05
|
|
|
disorganization, mouse, homolog of
|
[NCBI]
|
3.38675e-05
|
|
|
SHH
|
[NCBI]
|
3.291e-05
|
|
|
REN
|
[NCBI]
|
3.21844e-05
|
|
|
PFM
|
[NCBI]
|
3.15841e-05
|
|
|
OPD1
|
[NCBI]
|
3.15841e-05
|
|
|
multiple pterygium syndrome, escobar variant
|
[NCBI]
|
3.15841e-05
|
|
|
LRS1
|
[NCBI]
|
3.05645e-05
|
|
|
WHS
|
[NCBI]
|
3.02529e-05
|
|
|
CDH1
|
[NCBI]
|
2.7972e-05
|
|
|
PAX3
|
[NCBI]
|
2.58294e-05
|
|
|
MTR
|
[NCBI]
|
2.52113e-05
|
|
|
HS
|
[NCBI]
|
2.52113e-05
|
|
|
AFD1
|
[NCBI]
|
2.49549e-05
|
|
|
CPX
|
[NCBI]
|
2.43117e-05
|
|
|
CFNS
|
[NCBI]
|
2.09965e-05
|
|
|
SHFM1
|
[NCBI]
|
2.05957e-05
|
|
|
faciogenital dysplasia
|
[NCBI]
|
2.05179e-05
|
|
|
BOR1
|
[NCBI]
|
2.00568e-05
|
|
|
fraser syndrome
|
[NCBI]
|
2.00568e-05
|
|
|
SGBS1
|
[NCBI]
|
1.91826e-05
|
|
|
DA2A
|
[NCBI]
|
1.87676e-05
|
|
|
FGFR2
|
[NCBI]
|
1.82273e-05
|
|
|
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity
|
[NCBI]
|
1.79778e-05
|
|
|
MEB
|
[NCBI]
|
1.76016e-05
|
|
|
STL1
|
[NCBI]
|
1.72368e-05
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
1.72113e-05
|
|
|
OCA1A
|
[NCBI]
|
1.58819e-05
|
|
|
PHS
|
[NCBI]
|
1.55668e-05
|
|
|
BCNS
|
[NCBI]
|
1.45749e-05
|
|
|
CES
|
[NCBI]
|
1.33252e-05
|
|
|
TCOF
|
[NCBI]
|
1.011e-05
|
|
|
GNRH1
|
[NCBI]
|
9.96567e-06
|
|
|
NPS
|
[NCBI]
|
9.75345e-06
|
|
|
CCD
|
[NCBI]
|
7.34122e-06
|
|
|
NS1
|
[NCBI]
|
5.82653e-06
|
|
|
DBA
|
[NCBI]
|
3.74579e-06
|
|
|
EGFR
|
[NCBI]
|
1.22987e-06
|
|
|
DGS
|
[NCBI]
|
9.58104e-07
|
|