|
OMIM |
Link |
Information gain |
01 |
|
laurin-sandrow syndrome
|
[NCBI]
|
0.00354284
|
|
|
PHS
|
[NCBI]
|
0.00207752
|
|
|
SHH
|
[NCBI]
|
0.00124001
|
|
|
MKS2
|
[NCBI]
|
0.00119096
|
|
|
short rib-polydactyly syndrome, type i
|
[NCBI]
|
0.00113349
|
|
|
GCPS
|
[NCBI]
|
0.00113256
|
|
|
tibia, hypoplasia of, with polydactyly
|
[NCBI]
|
0.00100672
|
|
|
BBS
|
[NCBI]
|
0.00100091
|
|
|
short rib-polydactyly syndrome, type iii
|
[NCBI]
|
0.000973978
|
|
|
PPD2
|
[NCBI]
|
0.000973306
|
|
|
short rib-polydactyly syndrome, type iv
|
[NCBI]
|
0.000917517
|
|
|
polydactyly, postaxial, type a3
|
[NCBI]
|
0.000892148
|
|
|
polydactyly, postaxial, type a4
|
[NCBI]
|
0.000892148
|
|
|
camptosynpolydactyly, complex
|
[NCBI]
|
0.000892148
|
|
|
GLI3
|
[NCBI]
|
0.000891426
|
|
|
MKS1
|
[NCBI]
|
0.000788985
|
|
|
MKKS
|
[NCBI]
|
0.000745388
|
|
|
OFD3
|
[NCBI]
|
0.000592985
|
|
|
triphalangeal thumbs with brachyectrodactyly
|
[NCBI]
|
0.000592985
|
|
|
mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly
|
[NCBI]
|
0.000592985
|
|
|
ATD1
|
[NCBI]
|
0.000592469
|
|
|
SHFM1
|
[NCBI]
|
0.000576024
|
|
|
SPD1
|
[NCBI]
|
0.000563757
|
|
|
syndactyly, type i
|
[NCBI]
|
0.000500899
|
|
|
syndactyly, type i, with microcephaly and mental retardation
|
[NCBI]
|
0.000443979
|
|
|
brachyphalangy, polydactyly, and tibial aplasia/hypoplasia
|
[NCBI]
|
0.000422849
|
|
|
HOXD13
|
[NCBI]
|
0.000414506
|
|
|
polydactyly
|
[NCBI]
|
0.000382313
|
|
|
LMBR1
|
[NCBI]
|
0.000381414
|
|
|
OFD4
|
[NCBI]
|
0.000370612
|
|
|
constricting bands, congenital
|
[NCBI]
|
0.000332674
|
|
|
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging
|
[NCBI]
|
0.000332674
|
|
|
ACLS
|
[NCBI]
|
0.000323028
|
|
|
varadi-papp syndrome
|
[NCBI]
|
0.000321967
|
|
|
pseudotrisomy 13 syndrome
|
[NCBI]
|
0.00030613
|
|
|
SPD2
|
[NCBI]
|
0.000280511
|
|
|
cayler cardiofacial syndrome
|
[NCBI]
|
0.000263751
|
|
|
polydactyly, preaxial iv
|
[NCBI]
|
0.000262449
|
|
|
polydactyly, preaxial i
|
[NCBI]
|
0.000239553
|
|
|
polydactyly, postaxial, type a1
|
[NCBI]
|
0.000231275
|
|
|
holoprosencephaly
|
[NCBI]
|
0.000200419
|
|
|
DWS
|
[NCBI]
|
0.000174322
|
|
|
tibia, absence or hypoplasia of, with polydactyly, retrocerebellar arachnoid cyst, and other anomalies
|
[NCBI]
|
0.000105527
|
|
|
polydactyly, imperforate anus, and vertebral anomalies
|
[NCBI]
|
0.000105527
|
|
|
liver fibrocystic disease and polydactyly
|
[NCBI]
|
0.000105527
|
|
|
hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly
|
[NCBI]
|
0.000105527
|
|
|
ATD2
|
[NCBI]
|
0.000105527
|
|
|
preaxial hallucal polydactyly
|
[NCBI]
|
0.000105527
|
|
|
BBS4
|
[NCBI]
|
0.000101578
|
|
|
MKKS
|
[NCBI]
|
0.000101578
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
9.66969e-05
|
|
|
TBS
|
[NCBI]
|
8.58869e-05
|
|
|
EVC
|
[NCBI]
|
8.41813e-05
|
|
|
ulnar ray dysgenesis with postaxial polydactyly and renal cystic dysplasia
|
[NCBI]
|
8.30787e-05
|
|
|
MKS4
|
[NCBI]
|
8.30787e-05
|
|
|
preaxial deficiency, postaxial polydactyly, and hypospadias
|
[NCBI]
|
7.46206e-05
|
|
|
fibular aplasia, tibial campomelia, and oligosyndactyly syndrome
|
[NCBI]
|
7.46206e-05
|
|
|
RASSF8
|
[NCBI]
|
7.44041e-05
|
|
|
FBLN1
|
[NCBI]
|
7.44041e-05
|
|
|
IFT80
|
[NCBI]
|
7.44041e-05
|
|
|
DACH1
|
[NCBI]
|
7.44041e-05
|
|
|
KIAA0586
|
[NCBI]
|
7.44041e-05
|
|
|
PFM2
|
[NCBI]
|
6.91363e-05
|
|
|
cleft larynx, posterior
|
[NCBI]
|
6.18244e-05
|
|
|
weyers acrofacial dysostosis
|
[NCBI]
|
6.18244e-05
|
|
|
fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly
|
[NCBI]
|
6.18244e-05
|
|
|
MIPOL1
|
[NCBI]
|
6.06289e-05
|
|
|
ARIX
|
[NCBI]
|
6.06289e-05
|
|
|
IHH
|
[NCBI]
|
5.8743e-05
|
|
|
chondrodysplasia, grebe type
|
[NCBI]
|
5.3046e-05
|
|
|
hydrops-ectopic calcification-moth-eaten skeletal dysplasia
|
[NCBI]
|
5.3046e-05
|
|
|
char syndrome
|
[NCBI]
|
5.3046e-05
|
|
|
ARL6
|
[NCBI]
|
5.20607e-05
|
|
|
SMOH
|
[NCBI]
|
5.20607e-05
|
|
|
BBS2
|
[NCBI]
|
5.20607e-05
|
|
|
GLI2
|
[NCBI]
|
5.20607e-05
|
|
|
vater association
|
[NCBI]
|
5.14463e-05
|
|
|
FFS
|
[NCBI]
|
4.99946e-05
|
|
|
hydrolethalus syndrome 1
|
[NCBI]
|
4.99946e-05
|
|
|
HOXD3
|
[NCBI]
|
4.95545e-05
|
|
|
acheiropody
|
[NCBI]
|
4.86662e-05
|
|
|
hand-foot-uterus syndrome
|
[NCBI]
|
4.74421e-05
|
|
|
potocki-shaffer syndrome
|
[NCBI]
|
4.74421e-05
|
|
|
ACG2
|
[NCBI]
|
4.74421e-05
|
|
|
BDC
|
[NCBI]
|
4.63073e-05
|
|
|
GLI
|
[NCBI]
|
4.58994e-05
|
|
|
PROM1
|
[NCBI]
|
4.58994e-05
|
|
|
ALX4
|
[NCBI]
|
4.58994e-05
|
|
|
ZIC2
|
[NCBI]
|
4.58994e-05
|
|
|
TGIF
|
[NCBI]
|
4.58994e-05
|
|
|
SIX3
|
[NCBI]
|
4.448e-05
|
|
|
mulibrey nanism
|
[NCBI]
|
4.333e-05
|
|
|
EFNB1
|
[NCBI]
|
4.32397e-05
|
|
|
CEP290
|
[NCBI]
|
4.11483e-05
|
|
|
HOXA13
|
[NCBI]
|
4.11483e-05
|
|
|
SALL1
|
[NCBI]
|
4.02489e-05
|
|
|
MYBPC3
|
[NCBI]
|
3.73024e-05
|
|
|
USH1C
|
[NCBI]
|
3.61068e-05
|
|
|
PHOX2B
|
[NCBI]
|
3.55598e-05
|
|
|
DHCR7
|
[NCBI]
|
3.45502e-05
|
|
|
PTCH1
|
[NCBI]
|
3.40822e-05
|
|
|
MCOPS7
|
[NCBI]
|
3.36545e-05
|
|
|
immunodeficiency-centromeric instability-facial anomalies syndrome
|
[NCBI]
|
3.31872e-05
|
|
|
BMP2
|
[NCBI]
|
3.28002e-05
|
|
|
TWIST1
|
[NCBI]
|
3.2408e-05
|
|
|
GDF5
|
[NCBI]
|
3.20311e-05
|
|
|
BMP4
|
[NCBI]
|
3.03405e-05
|
|
|
FDH
|
[NCBI]
|
2.88489e-05
|
|
|
AVSD
|
[NCBI]
|
1.94165e-05
|
|
|
FGFR2
|
[NCBI]
|
1.64824e-05
|
|
|
GFAP
|
[NCBI]
|
9.23651e-06
|
|
|
SLOS
|
[NCBI]
|
7.1461e-06
|
|
|
EGFR
|
[NCBI]
|
2.62081e-06
|
|
|
TH
|
[NCBI]
|
4.72664e-07
|
|
|
RP
|
[NCBI]
|
2.53515e-09
|
|