|
OMIM |
Link |
Information gain |
01 |
|
poland syndrome
|
[NCBI]
|
0.00987441
|
|
|
cenani syndactylism
|
[NCBI]
|
0.00390963
|
|
|
syndactyly, type i, with microcephaly and mental retardation
|
[NCBI]
|
0.00325328
|
|
|
syndactyly, type i
|
[NCBI]
|
0.00273043
|
|
|
GCPS
|
[NCBI]
|
0.00163111
|
|
|
laurin-sandrow syndrome
|
[NCBI]
|
0.0014442
|
|
|
tibia, hypoplasia of, with polydactyly
|
[NCBI]
|
0.00138553
|
|
|
SPD1
|
[NCBI]
|
0.00132055
|
|
|
ODDD
|
[NCBI]
|
0.00122205
|
|
|
rosselli-gulienetti syndrome
|
[NCBI]
|
0.00112277
|
|
|
fraser syndrome
|
[NCBI]
|
0.000779586
|
|
|
synpolydactyly 3
|
[NCBI]
|
0.000777045
|
|
|
BDA4
|
[NCBI]
|
0.000777045
|
|
|
MSSD
|
[NCBI]
|
0.000777045
|
|
|
HOXD13
|
[NCBI]
|
0.000616983
|
|
|
blepharophimosis with ptosis, syndactyly, and short stature
|
[NCBI]
|
0.000560203
|
|
|
polysyndactyly, crossed
|
[NCBI]
|
0.000560203
|
|
|
CRSA
|
[NCBI]
|
0.000560203
|
|
|
hypertelorism, microtia, facial clefting syndrome
|
[NCBI]
|
0.000426747
|
|
|
oculodentoosseous dysplasia, recessive
|
[NCBI]
|
0.000426747
|
|
|
SPD2
|
[NCBI]
|
0.000403333
|
|
|
kbg syndrome
|
[NCBI]
|
0.000388139
|
|
|
PPS
|
[NCBI]
|
0.000382818
|
|
|
CLPED1
|
[NCBI]
|
0.000381725
|
|
|
PPD2
|
[NCBI]
|
0.000372497
|
|
|
SHFM1
|
[NCBI]
|
0.000364291
|
|
|
OSCS
|
[NCBI]
|
0.000357599
|
|
|
AOS
|
[NCBI]
|
0.000343086
|
|
|
syndactyly, type iii
|
[NCBI]
|
0.000341487
|
|
|
SOST
|
[NCBI]
|
0.000322556
|
|
|
digeorge syndrome/velocardiofacial syndrome spectrum of malformation 2
|
[NCBI]
|
0.000310971
|
|
|
klippel-feil syndrome, autosomal dominant
|
[NCBI]
|
0.000310971
|
|
|
popliteal pterygium syndrome, lethal type
|
[NCBI]
|
0.000310971
|
|
|
blepharocheilodontic syndrome
|
[NCBI]
|
0.000310971
|
|
|
SHFLD1
|
[NCBI]
|
0.000248175
|
|
|
LRP4
|
[NCBI]
|
0.000239952
|
|
|
mohr syndrome
|
[NCBI]
|
0.00022519
|
|
|
short rib-polydactyly syndrome, type ii
|
[NCBI]
|
0.0002057
|
|
|
syndactyly, type iv
|
[NCBI]
|
0.000201484
|
|
|
arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly
|
[NCBI]
|
0.000201484
|
|
|
polysyndactyly with cardiac malformation
|
[NCBI]
|
0.000201484
|
|
|
scott craniodigital syndrome with mental retardation
|
[NCBI]
|
0.000201484
|
|
|
syndactyly, type v
|
[NCBI]
|
0.000201484
|
|
|
apert syndrome
|
[NCBI]
|
0.000198933
|
|
|
megalencephaly-cutis marmorata telangiectatica congenita
|
[NCBI]
|
0.000198134
|
|
|
schinzel-giedion midface-retraction syndrome
|
[NCBI]
|
0.000196987
|
|
|
ACC
|
[NCBI]
|
0.000196987
|
|
|
PHS
|
[NCBI]
|
0.000187323
|
|
|
GJA1
|
[NCBI]
|
0.000177856
|
|
|
acrofrontofacionasal dysostosis, severe
|
[NCBI]
|
0.000170561
|
|
|
robinow syndrome, autosomal recessive
|
[NCBI]
|
0.000160923
|
|
|
eem syndrome
|
[NCBI]
|
0.000156603
|
|
|
TS
|
[NCBI]
|
0.000156603
|
|
|
GLI3
|
[NCBI]
|
0.000150128
|
|
|
dubowitz syndrome
|
[NCBI]
|
0.000149215
|
|
|
FGFR2
|
[NCBI]
|
0.000141674
|
|
|
NLS
|
[NCBI]
|
0.000138613
|
|
|
FDH
|
[NCBI]
|
0.00012504
|
|
|
SLOS
|
[NCBI]
|
0.000124041
|
|
|
SHH
|
[NCBI]
|
0.000106487
|
|
|
EEC1
|
[NCBI]
|
0.000101175
|
|
|
hallux varus and preaxial polysyndactyly
|
[NCBI]
|
0.000100696
|
|
|
aurocephalosyndactyly
|
[NCBI]
|
0.000100696
|
|
|
brachydactyly-syndactyly syndrome
|
[NCBI]
|
0.000100696
|
|
|
dauwerse-peters syndrome
|
[NCBI]
|
0.000100696
|
|
|
odontotrichoungual-digital-palmar syndrome
|
[NCBI]
|
0.000100696
|
|
|
ectodermal dysplasia with mental retardation and syndactyly
|
[NCBI]
|
0.000100696
|
|
|
syndactyly with renal and anogenital malformations
|
[NCBI]
|
0.000100696
|
|
|
acrorenal syndrome
|
[NCBI]
|
0.000100696
|
|
|
ackerman syndrome
|
[NCBI]
|
0.000100696
|
|
|
radioulnar synostosis, radial ray abnormalities, and severe malformations in the male
|
[NCBI]
|
0.000100696
|
|
|
polydactyly, postaxial, with dental and vertebral anomalies
|
[NCBI]
|
0.000100696
|
|
|
symphalangism with multiple anomalies of hands and feet
|
[NCBI]
|
0.000100696
|
|
|
ROR2
|
[NCBI]
|
9.98716e-05
|
|
|
DHCR7
|
[NCBI]
|
9.41614e-05
|
|
|
DWS
|
[NCBI]
|
8.26981e-05
|
|
|
FLNA
|
[NCBI]
|
8.252e-05
|
|
|
contractural arachnodactyly, congenital
|
[NCBI]
|
8.252e-05
|
|
|
RASSF8
|
[NCBI]
|
7.97709e-05
|
|
|
FBLN1
|
[NCBI]
|
7.97709e-05
|
|
|
MBOAT1
|
[NCBI]
|
7.97709e-05
|
|
|
mental retardation, x-linked, with short stature
|
[NCBI]
|
7.97709e-05
|
|
|
pterygium syndrome, multiple, autosomal dominant
|
[NCBI]
|
7.82562e-05
|
|
|
second metatarsal-metacarpal syndrome
|
[NCBI]
|
7.82562e-05
|
|
|
acrofrontofacionasal dysostosis syndrome
|
[NCBI]
|
7.82562e-05
|
|
|
cleft palate, cardiac defect, genital anomalies, and ectrodactyly
|
[NCBI]
|
7.82562e-05
|
|
|
RBS
|
[NCBI]
|
7.5631e-05
|
|
|
cree mental retardation syndrome
|
[NCBI]
|
6.98065e-05
|
|
|
alopecia-contractures-dwarfism mental retardation syndrome
|
[NCBI]
|
6.98065e-05
|
|
|
polydactyly, postaxial
|
[NCBI]
|
6.98065e-05
|
|
|
preaxial deficiency, postaxial polydactyly, and hypospadias
|
[NCBI]
|
6.98065e-05
|
|
|
ankyloblepharon filiforme adnatum and cleft palate
|
[NCBI]
|
6.98065e-05
|
|
|
split-foot deformity with mandibulofacial dysostosis
|
[NCBI]
|
6.98065e-05
|
|
|
scalp defects and postaxial polydactyly
|
[NCBI]
|
6.98065e-05
|
|
|
brachydactyly-ectrodactyly with fibular aplasia or hypoplasia
|
[NCBI]
|
6.98065e-05
|
|
|
multiple pterygium syndrome, aslan type
|
[NCBI]
|
6.98065e-05
|
|
|
mental retardation, buenos aires type
|
[NCBI]
|
6.98065e-05
|
|
|
FGFR1
|
[NCBI]
|
6.55916e-05
|
|
|
humerospinal dysostosis
|
[NCBI]
|
6.43307e-05
|
|
|
IDH3G
|
[NCBI]
|
6.07951e-05
|
|
|
FREM2
|
[NCBI]
|
6.07951e-05
|
|
|
femur-fibula-ulna syndrome
|
[NCBI]
|
6.02672e-05
|
|
|
scalp-ear-nipple syndrome
|
[NCBI]
|
6.02672e-05
|
|
|
SLC12A2
|
[NCBI]
|
5.74205e-05
|
|
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
5.72762e-05
|
|
|
cleft lip/palate with abnormal thumbs and microcephaly
|
[NCBI]
|
5.70355e-05
|
|
|
neuroblastoma stage 4s gene
|
[NCBI]
|
5.4912e-05
|
|
|
HOXD3
|
[NCBI]
|
5.4912e-05
|
|
|
BDE
|
[NCBI]
|
5.20623e-05
|
|
|
ACY1
|
[NCBI]
|
5.12523e-05
|
|
|
PVRL1
|
[NCBI]
|
4.85879e-05
|
|
|
LMBR1
|
[NCBI]
|
4.74843e-05
|
|
|
JWS
|
[NCBI]
|
4.66993e-05
|
|
|
HOXA13
|
[NCBI]
|
4.64918e-05
|
|
|
IKZF1
|
[NCBI]
|
4.55901e-05
|
|
|
kindler syndrome
|
[NCBI]
|
4.52561e-05
|
|
|
hyperostosis corticalis generalisata
|
[NCBI]
|
4.52561e-05
|
|
|
CRS1
|
[NCBI]
|
4.39361e-05
|
|
|
LADD
|
[NCBI]
|
4.39361e-05
|
|
|
three m syndrome
|
[NCBI]
|
4.39361e-05
|
|
|
hand-foot-uterus syndrome
|
[NCBI]
|
4.27203e-05
|
|
|
MCOPS2
|
[NCBI]
|
4.27203e-05
|
|
|
MYBPC3
|
[NCBI]
|
4.26343e-05
|
|
|
OPD1
|
[NCBI]
|
4.15939e-05
|
|
|
c syndrome
|
[NCBI]
|
4.15939e-05
|
|
|
feingold syndrome
|
[NCBI]
|
4.15939e-05
|
|
|
PHOX2B
|
[NCBI]
|
4.08847e-05
|
|
|
EEC3
|
[NCBI]
|
3.95635e-05
|
|
|
heterotopia, periventricular, x-linked dominant
|
[NCBI]
|
3.95635e-05
|
|
|
FMD
|
[NCBI]
|
3.86418e-05
|
|
|
BMP2
|
[NCBI]
|
3.81111e-05
|
|
|
TWIST1
|
[NCBI]
|
3.77166e-05
|
|
|
MNS
|
[NCBI]
|
3.47293e-05
|
|
|
HSS
|
[NCBI]
|
3.40568e-05
|
|
|
HNA
|
[NCBI]
|
3.40568e-05
|
|
|
ACLS
|
[NCBI]
|
3.27975e-05
|
|
|
OFD1
|
[NCBI]
|
3.16382e-05
|
|
|
OKS
|
[NCBI]
|
3.0565e-05
|
|
|
SCDO1
|
[NCBI]
|
2.90922e-05
|
|
|
MCOPS7
|
[NCBI]
|
2.90922e-05
|
|
|
charge syndrome
|
[NCBI]
|
2.69347e-05
|
|
|
SPG3A
|
[NCBI]
|
2.61573e-05
|
|
|
TRPS2
|
[NCBI]
|
2.50679e-05
|
|
|
COH1
|
[NCBI]
|
2.50679e-05
|
|
|
SCS
|
[NCBI]
|
2.43874e-05
|
|
|
HNPP
|
[NCBI]
|
2.14259e-05
|
|
|
FGFR3
|
[NCBI]
|
1.65716e-05
|
|
|
DGS
|
[NCBI]
|
6.05075e-06
|
|
|
MFS
|
[NCBI]
|
3.04044e-06
|
|
|
EGFR
|
[NCBI]
|
6.00187e-08
|
|