|
OMIM |
Link |
Information gain |
01 |
|
amelogenesis imperfecta, hypoplastic type
|
[NCBI]
|
0.0012742
|
|
|
dentin dysplasia, type i
|
[NCBI]
|
0.00108094
|
|
|
molar i reinclusion
|
[NCBI]
|
0.00102443
|
|
|
EEC1
|
[NCBI]
|
0.000621935
|
|
|
DGI1
|
[NCBI]
|
0.000612831
|
|
|
kabuki syndrome
|
[NCBI]
|
0.000526903
|
|
|
dentinogenesis imperfecta, shields type iii
|
[NCBI]
|
0.000480476
|
|
|
HFM
|
[NCBI]
|
0.00047322
|
|
|
steatocystoma multiplex with natal teeth
|
[NCBI]
|
0.00042739
|
|
|
teeth present at birth
|
[NCBI]
|
0.000373303
|
|
|
periodontitis, aggressive, 1
|
[NCBI]
|
0.00026942
|
|
|
hypophosphatasia, infantile
|
[NCBI]
|
0.000240547
|
|
|
ACP5
|
[NCBI]
|
0.000214875
|
|
|
intestinal pseudoobstruction with patent ductus arteriosus and natal teeth
|
[NCBI]
|
0.000213171
|
|
|
osteogenesis imperfecta with opalescent teeth
|
[NCBI]
|
0.000213171
|
|
|
RSTS
|
[NCBI]
|
0.000202963
|
|
|
CCD
|
[NCBI]
|
0.000174389
|
|
|
PC2
|
[NCBI]
|
0.000159098
|
|
|
CPI
|
[NCBI]
|
0.000154496
|
|
|
witkop syndrome
|
[NCBI]
|
0.000149486
|
|
|
intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked
|
[NCBI]
|
0.000131923
|
|
|
dentin dysplasia, type ii
|
[NCBI]
|
0.000131923
|
|
|
kindler syndrome
|
[NCBI]
|
0.000131923
|
|
|
ALSG
|
[NCBI]
|
0.000115814
|
|
|
SMMCI
|
[NCBI]
|
0.000102444
|
|
|
EVC
|
[NCBI]
|
9.34556e-05
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
8.66877e-05
|
|
|
DSPP
|
[NCBI]
|
7.27748e-05
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
7.138e-05
|
|
|
TNFRSF11B
|
[NCBI]
|
6.67061e-05
|
|
|
WHS
|
[NCBI]
|
5.97643e-05
|
|
|
SPP1
|
[NCBI]
|
3.55125e-05
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
1.60681e-05
|
|
|
CF
|
[NCBI]
|
8.29466e-06
|
|
|
PTH
|
[NCBI]
|
3.69664e-06
|
|
|
NPY
|
[NCBI]
|
3.06151e-06
|
|
|
EGF
|
[NCBI]
|
1.64094e-07
|
|