|
OMIM |
Link |
Information gain |
01 |
|
kbg syndrome
|
[NCBI]
|
0.00397413
|
|
|
blepharocheilodontic syndrome
|
[NCBI]
|
0.00314491
|
|
|
STHAG4
|
[NCBI]
|
0.00242527
|
|
|
RIEG2
|
[NCBI]
|
0.00202379
|
|
|
robinow syndrome, autosomal dominant
|
[NCBI]
|
0.00165122
|
|
|
cranioectodermal dysplasia
|
[NCBI]
|
0.00154932
|
|
|
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth
|
[NCBI]
|
0.00148175
|
|
|
oculodentoosseous dysplasia, recessive
|
[NCBI]
|
0.00114777
|
|
|
ODDD
|
[NCBI]
|
0.00106575
|
|
|
kabuki syndrome
|
[NCBI]
|
0.00098122
|
|
|
EEC1
|
[NCBI]
|
0.000798777
|
|
|
STHAG2
|
[NCBI]
|
0.00078953
|
|
|
microcephalic osteodysplastic primordial dwarfism with tooth abnormalities
|
[NCBI]
|
0.00078953
|
|
|
trichodentoosseous syndrome
|
[NCBI]
|
0.00078592
|
|
|
NHS
|
[NCBI]
|
0.000748016
|
|
|
microcephalic osteodysplastic primordial dwarfism, type ii
|
[NCBI]
|
0.00074174
|
|
|
otodental dysplasia
|
[NCBI]
|
0.000572601
|
|
|
teeth, odd shapes of
|
[NCBI]
|
0.000572601
|
|
|
cerebrooculonasal syndrome
|
[NCBI]
|
0.000572601
|
|
|
STHAG5
|
[NCBI]
|
0.000572601
|
|
|
HFH
|
[NCBI]
|
0.000572601
|
|
|
PRS
|
[NCBI]
|
0.000572601
|
|
|
IP
|
[NCBI]
|
0.000513152
|
|
|
RIEG1
|
[NCBI]
|
0.000506533
|
|
|
axenfeld-rieger anomaly with cardiac defects and sensorineural hearing loss
|
[NCBI]
|
0.000491365
|
|
|
cone-rod dystrophy and amelogenesis imperfecta
|
[NCBI]
|
0.000491365
|
|
|
ED1
|
[NCBI]
|
0.000482155
|
|
|
weyers acrofacial dysostosis
|
[NCBI]
|
0.000441477
|
|
|
anodontia of permanent dentition
|
[NCBI]
|
0.000438973
|
|
|
LADD
|
[NCBI]
|
0.000437362
|
|
|
HTC2
|
[NCBI]
|
0.000400278
|
|
|
molar i reinclusion
|
[NCBI]
|
0.000400278
|
|
|
dentin dysplasia, type i
|
[NCBI]
|
0.000400278
|
|
|
taurodontism
|
[NCBI]
|
0.000388063
|
|
|
EVC
|
[NCBI]
|
0.000383622
|
|
|
hypertrichosis universalis
|
[NCBI]
|
0.000369652
|
|
|
maxillonasal dysplasia, binder type
|
[NCBI]
|
0.000369652
|
|
|
HSS
|
[NCBI]
|
0.000364473
|
|
|
syndactyly, type i, with microcephaly and mental retardation
|
[NCBI]
|
0.000344358
|
|
|
HBD
|
[NCBI]
|
0.000344358
|
|
|
GO
|
[NCBI]
|
0.00030418
|
|
|
HTC1
|
[NCBI]
|
0.00030418
|
|
|
acrodysostosis
|
[NCBI]
|
0.00030418
|
|
|
DA5
|
[NCBI]
|
0.000287707
|
|
|
MCOPS2
|
[NCBI]
|
0.000252691
|
|
|
mohr syndrome
|
[NCBI]
|
0.000236553
|
|
|
DLX3
|
[NCBI]
|
0.000235768
|
|
|
AIHHT
|
[NCBI]
|
0.000223642
|
|
|
JBS
|
[NCBI]
|
0.00021358
|
|
|
dermoodontodysplasia
|
[NCBI]
|
0.000193887
|
|
|
ectodermal dysplasia, trichoodontoonychial type
|
[NCBI]
|
0.000193887
|
|
|
deafness, congenital, with inner ear agenesis, microtia, and microdontia
|
[NCBI]
|
0.000193887
|
|
|
carabelli anomaly of maxillary molar teeth
|
[NCBI]
|
0.000193887
|
|
|
NHS
|
[NCBI]
|
0.000188263
|
|
|
adult syndrome
|
[NCBI]
|
0.000177504
|
|
|
FDH
|
[NCBI]
|
0.000170909
|
|
|
GJA1
|
[NCBI]
|
0.000170815
|
|
|
EEC3
|
[NCBI]
|
0.000163088
|
|
|
gorlin-chaudhry-moss syndrome
|
[NCBI]
|
0.000162973
|
|
|
codas syndrome
|
[NCBI]
|
0.000162973
|
|
|
SMMCI
|
[NCBI]
|
0.000157251
|
|
|
MSX1
|
[NCBI]
|
0.000157068
|
|
|
RHS
|
[NCBI]
|
0.000152058
|
|
|
OODD
|
[NCBI]
|
0.000149023
|
|
|
oroacral syndrome, verloes-koulischer type
|
[NCBI]
|
0.000149023
|
|
|
PITX2
|
[NCBI]
|
0.000143419
|
|
|
scalp-ear-nipple syndrome
|
[NCBI]
|
0.00013946
|
|
|
CCD
|
[NCBI]
|
0.00012987
|
|
|
ichthyosiform erythroderma, corneal involvement, and deafness
|
[NCBI]
|
0.000126203
|
|
|
HMI
|
[NCBI]
|
0.000125679
|
|
|
EVC
|
[NCBI]
|
0.000123552
|
|
|
ALSG
|
[NCBI]
|
0.000121206
|
|
|
dentinogenesis imperfecta, shields type iii
|
[NCBI]
|
0.000113095
|
|
|
PAX9
|
[NCBI]
|
0.000107278
|
|
|
IRID2
|
[NCBI]
|
0.000106649
|
|
|
LMS
|
[NCBI]
|
9.89357e-05
|
|
|
ectodermal dysplasia with natal teeth, turnpenny type
|
[NCBI]
|
9.69075e-05
|
|
|
pilodental dysplasia with refractive errors
|
[NCBI]
|
9.69075e-05
|
|
|
ectodermal dysplasia with adrenal cyst
|
[NCBI]
|
9.69075e-05
|
|
|
odontomicronychial dysplasia
|
[NCBI]
|
9.69075e-05
|
|
|
ectodermal dysplasia with mental retardation and syndactyly
|
[NCBI]
|
9.69075e-05
|
|
|
dens in dente and palatal invaginations
|
[NCBI]
|
9.69075e-05
|
|
|
teeth, noneruption of, with maxillary hypoplasia and genu valgum
|
[NCBI]
|
9.69075e-05
|
|
|
teeth, congenital absence of, with taurodontia and sparse hair
|
[NCBI]
|
9.69075e-05
|
|
|
spondyloepimetaphyseal dysplasia with abnormal dentition
|
[NCBI]
|
9.69075e-05
|
|
|
dental noneruption
|
[NCBI]
|
9.69075e-05
|
|
|
symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch
|
[NCBI]
|
9.69075e-05
|
|
|
incisors, lower central, absence of
|
[NCBI]
|
9.69075e-05
|
|
|
xanthinuria, type ii
|
[NCBI]
|
9.69075e-05
|
|
|
ackerman syndrome
|
[NCBI]
|
9.69075e-05
|
|
|
polydactyly, postaxial, with dental and vertebral anomalies
|
[NCBI]
|
9.69075e-05
|
|
|
corneodermatoosseous syndrome
|
[NCBI]
|
9.69075e-05
|
|
|
incisors, shovel-shaped
|
[NCBI]
|
9.69075e-05
|
|
|
taurodontism, microdontia, and dens invaginatus
|
[NCBI]
|
9.69075e-05
|
|
|
growth retardation, small and puffy hands and feet, and eczema
|
[NCBI]
|
9.69075e-05
|
|
|
hypoplasia of teeth roots
|
[NCBI]
|
9.69075e-05
|
|
|
STHAGX1
|
[NCBI]
|
9.69075e-05
|
|
|
FOXC1
|
[NCBI]
|
9.46333e-05
|
|
|
EDA
|
[NCBI]
|
9.24269e-05
|
|
|
immunoosseous dysplasia, schimke type
|
[NCBI]
|
9.09403e-05
|
|
|
OPTB3
|
[NCBI]
|
8.76029e-05
|
|
|
OFD1
|
[NCBI]
|
7.81531e-05
|
|
|
andersen cardiodysrhythmic periodic paralysis
|
[NCBI]
|
7.70144e-05
|
|
|
aredyld
|
[NCBI]
|
7.44759e-05
|
|
|
pallister w syndrome
|
[NCBI]
|
7.44759e-05
|
|
|
temtamy preaxial brachydactyly syndrome
|
[NCBI]
|
7.44759e-05
|
|
|
telecanthus
|
[NCBI]
|
7.44759e-05
|
|
|
tooth size
|
[NCBI]
|
7.44759e-05
|
|
|
deafness-oligodontia syndrome
|
[NCBI]
|
7.44759e-05
|
|
|
tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities
|
[NCBI]
|
7.44759e-05
|
|
|
tooth malformation
|
[NCBI]
|
7.44759e-05
|
|
|
trichodental dysplasia
|
[NCBI]
|
7.44759e-05
|
|
|
mucopolysaccharidosis type iva
|
[NCBI]
|
7.25221e-05
|
|
|
PAX6
|
[NCBI]
|
7.03726e-05
|
|
|
neurofaciodigitorenal syndrome
|
[NCBI]
|
6.60348e-05
|
|
|
steatocystoma multiplex with natal teeth
|
[NCBI]
|
6.60348e-05
|
|
|
bone fragility with craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features
|
[NCBI]
|
6.60348e-05
|
|
|
CRMP1
|
[NCBI]
|
6.46273e-05
|
|
|
epidermolysis bullosa, late-onset localized junctional, with mental retardation
|
[NCBI]
|
6.05675e-05
|
|
|
coloboma of macula with type b brachydactyly
|
[NCBI]
|
6.05675e-05
|
|
|
robin sequence with cleft mandible and limb anomalies
|
[NCBI]
|
6.05675e-05
|
|
|
DYNLL1
|
[NCBI]
|
5.94295e-05
|
|
|
splenogonadal fusion with limb defects and micrognathia
|
[NCBI]
|
5.65125e-05
|
|
|
ED3
|
[NCBI]
|
5.65125e-05
|
|
|
BCOR
|
[NCBI]
|
5.60554e-05
|
|
|
EYA2
|
[NCBI]
|
5.60554e-05
|
|
|
DKK1
|
[NCBI]
|
5.35473e-05
|
|
|
weyers ulnar ray/oligodactyly syndrome
|
[NCBI]
|
5.32895e-05
|
|
|
STHAG1
|
[NCBI]
|
5.32895e-05
|
|
|
syndactyly, type iii
|
[NCBI]
|
5.32895e-05
|
|
|
peters anomaly
|
[NCBI]
|
5.32895e-05
|
|
|
witkop syndrome
|
[NCBI]
|
5.32895e-05
|
|
|
RSTS
|
[NCBI]
|
5.31124e-05
|
|
|
STHAG3
|
[NCBI]
|
5.06161e-05
|
|
|
anonychia congenita
|
[NCBI]
|
5.06161e-05
|
|
|
EVC2
|
[NCBI]
|
4.98886e-05
|
|
|
dentin dysplasia, type ii
|
[NCBI]
|
4.83334e-05
|
|
|
GALNT3
|
[NCBI]
|
4.72252e-05
|
|
|
FGF10
|
[NCBI]
|
4.72252e-05
|
|
|
SOX3
|
[NCBI]
|
4.72252e-05
|
|
|
FGF3
|
[NCBI]
|
4.61221e-05
|
|
|
MSX2
|
[NCBI]
|
4.513e-05
|
|
|
BDB1
|
[NCBI]
|
4.45789e-05
|
|
|
weill-marchesani syndrome, autosomal recessive
|
[NCBI]
|
4.45789e-05
|
|
|
KCNJ2
|
[NCBI]
|
4.26414e-05
|
|
|
WHS
|
[NCBI]
|
4.16876e-05
|
|
|
chromosome 18q deletion syndrome
|
[NCBI]
|
4.15615e-05
|
|
|
SALL4
|
[NCBI]
|
4.12749e-05
|
|
|
ROR2
|
[NCBI]
|
4.12749e-05
|
|
|
PQBP1
|
[NCBI]
|
4.06569e-05
|
|
|
HPE2
|
[NCBI]
|
3.9043e-05
|
|
|
PC1
|
[NCBI]
|
3.9043e-05
|
|
|
TCOF1
|
[NCBI]
|
3.80436e-05
|
|
|
cerebrocostomandibular syndrome
|
[NCBI]
|
3.79251e-05
|
|
|
PFM
|
[NCBI]
|
3.79251e-05
|
|
|
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 1
|
[NCBI]
|
3.79251e-05
|
|
|
HPE3
|
[NCBI]
|
3.79251e-05
|
|
|
LRS1
|
[NCBI]
|
3.68846e-05
|
|
|
xanthinuria, type i
|
[NCBI]
|
3.68846e-05
|
|
|
DGI1
|
[NCBI]
|
3.68846e-05
|
|
|
TP73L
|
[NCBI]
|
3.6756e-05
|
|
|
ALPL
|
[NCBI]
|
3.6362e-05
|
|
|
spondyloepimetaphyseal dysplasia, strudwick type
|
[NCBI]
|
3.49988e-05
|
|
|
DRRS
|
[NCBI]
|
3.49988e-05
|
|
|
ED2
|
[NCBI]
|
3.49988e-05
|
|
|
keratitis-ichthyosis-deafness syndrome, autosomal dominant
|
[NCBI]
|
3.49988e-05
|
|
|
COL17A1
|
[NCBI]
|
3.46004e-05
|
|
|
KFSD
|
[NCBI]
|
3.41388e-05
|
|
|
crouzon syndrome
|
[NCBI]
|
3.33262e-05
|
|
|
UMS
|
[NCBI]
|
3.33262e-05
|
|
|
ichthyosis congenita, harlequin fetus type
|
[NCBI]
|
3.25564e-05
|
|
|
PALS
|
[NCBI]
|
3.25564e-05
|
|
|
robinow syndrome, autosomal recessive
|
[NCBI]
|
3.18252e-05
|
|
|
GABEB
|
[NCBI]
|
3.11292e-05
|
|
|
weaver syndrome
|
[NCBI]
|
3.04652e-05
|
|
|
leopard syndrome 1
|
[NCBI]
|
2.65255e-05
|
|
|
HFTC
|
[NCBI]
|
2.65255e-05
|
|
|
HFM
|
[NCBI]
|
2.61747e-05
|
|
|
PKS
|
[NCBI]
|
2.55779e-05
|
|
|
MITF
|
[NCBI]
|
2.52579e-05
|
|
|
COH1
|
[NCBI]
|
2.16395e-05
|
|
|
WBS
|
[NCBI]
|
2.05436e-05
|
|
|
RTS
|
[NCBI]
|
1.78468e-05
|
|
|
WS1
|
[NCBI]
|
1.66537e-05
|
|
|
VWS
|
[NCBI]
|
1.6429e-05
|
|
|
TCOF
|
[NCBI]
|
1.53673e-05
|
|
|
HGPS
|
[NCBI]
|
1.36792e-05
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
1.22232e-05
|
|
|
SHH
|
[NCBI]
|
1.20766e-05
|
|
|
SDS
|
[NCBI]
|
1.13576e-05
|
|
|
NS1
|
[NCBI]
|
1.04374e-05
|
|
|
APS1
|
[NCBI]
|
9.71584e-06
|
|
|
SMS
|
[NCBI]
|
9.48775e-06
|
|
|
SPP1
|
[NCBI]
|
6.91249e-06
|
|
|
EGF
|
[NCBI]
|
4.84802e-06
|
|
|
BCNS
|
[NCBI]
|
4.37767e-06
|
|
|
APC
|
[NCBI]
|
2.7363e-06
|
|
|
SRS
|
[NCBI]
|
2.59193e-06
|
|
|
SLOS
|
[NCBI]
|
2.2652e-06
|
|
|
MFS
|
[NCBI]
|
1.40825e-06
|
|
|
FA
|
[NCBI]
|
1.35994e-06
|
|
|
PTH
|
[NCBI]
|
8.31227e-07
|
|
|
BWS
|
[NCBI]
|
3.77995e-07
|
|