|
OMIM |
Link |
Information
gain |
01 |
|
|
kenny-caffey syndrome, type 2
|
[NCBI]
|
0.00324374
|
|
|
|
caffey disease
|
[NCBI]
|
0.00130808
|
|
|
|
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus
|
[NCBI]
|
0.000814336
|
|
|
|
hyperostosis corticalis generalisata
|
[NCBI]
|
0.000394694
|
|
|
|
HHS
|
[NCBI]
|
0.000173657
|
|
|
|
paget disease, juvenile
|
[NCBI]
|
0.000160509
|
|
|
|
calvarial hyperostosis
|
[NCBI]
|
0.000128816
|
|
|
|
COL1A1
|
[NCBI]
|
0.000117393
|
|
|
|
van buchem disease, type 2
|
[NCBI]
|
0.000106349
|
|
|
|
SOST
|
[NCBI]
|
7.34161e-05
|
|
|
|
FMD
|
[NCBI]
|
6.63057e-05
|
|
|
|
SOST
|
[NCBI]
|
6.45623e-05
|
|
|
|
WAS
|
[NCBI]
|
6.44114e-05
|
|
|
|
camurati-engelmann disease
|
[NCBI]
|
5.7907e-05
|
|
|
|
HFTC
|
[NCBI]
|
5.73722e-05
|
|
|
|
phenylketonuria
|
[NCBI]
|
4.20174e-05
|
|
