|
OMIM |
Link |
Information
gain |
01 |
|
|
APC
|
[NCBI]
|
0.00136884
|
|
|
|
osseous heteroplasia, progressive
|
[NCBI]
|
0.000175181
|
|
|
|
osteoma of cranial vault, familial
|
[NCBI]
|
0.000125989
|
|
|
|
osteoma of middle ear
|
[NCBI]
|
0.000125989
|
|
|
|
choroidal osteoma, bilateral
|
[NCBI]
|
0.000103524
|
|
|
|
dysplasia epiphysealis hemimelica
|
[NCBI]
|
9.50481e-05
|
|
|
|
opitz syndrome
|
[NCBI]
|
7.33522e-05
|
|
|
|
PXE
|
[NCBI]
|
6.7798e-05
|
|
|
|
enchondromatosis, multiple
|
[NCBI]
|
6.44451e-05
|
|
|
|
apc gene
|
[NCBI]
|
5.45363e-05
|
|
|
|
MTS
|
[NCBI]
|
4.21849e-05
|
|
|
|
lynch syndrome i
|
[NCBI]
|
3.97776e-05
|
|
|
|
AHO
|
[NCBI]
|
3.58753e-05
|
|
|
|
PTH
|
[NCBI]
|
2.25605e-05
|
|
|
|
MJD
|
[NCBI]
|
2.13609e-05
|
|
