|
OMIM |
Link |
Information
gain |
01 |
|
|
osteolysis, hereditary, of carpal bones with nephropathy
|
[NCBI]
|
0.00805838
|
|
|
|
acroosteolysis with osteoporosis and changes in skull and mandible
|
[NCBI]
|
0.00469419
|
|
|
|
hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
|
[NCBI]
|
0.00100366
|
|
|
|
cystic angiomatosis of bone, diffuse
|
[NCBI]
|
0.000255404
|
|
|
|
serpentine fibula-polycystic kidney syndrome
|
[NCBI]
|
0.00020909
|
|
|
|
winchester syndrome
|
[NCBI]
|
0.00020909
|
|
|
|
MMP2
|
[NCBI]
|
0.000160618
|
|
|
|
osteolysis syndrome, recessive
|
[NCBI]
|
0.000142554
|
|
|
|
expansile bone lesions
|
[NCBI]
|
0.000142554
|
|
|
|
osteolysis, hereditary multicentric
|
[NCBI]
|
0.000102005
|
|
|
|
MONA
|
[NCBI]
|
9.87429e-05
|
|
|
|
fibromatosis, juvenile hyaline
|
[NCBI]
|
8.54328e-05
|
|
|
|
HEPOD
|
[NCBI]
|
7.74297e-05
|
|
|
|
CRMO
|
[NCBI]
|
5.89513e-05
|
|
|
|
RA
|
[NCBI]
|
7.69029e-06
|
|
