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MeSH keywords -> Related genes, diseases (OMIM)


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01 Osteolysis, Essential [NCBI]

Gene


 Gene Link Information
Gain		 01
TNFRSF11A [NCBI] 4.25809e-05
TNFSF11 [NCBI] 4.16172e-05
PSTPIP2 [NCBI] 1.81191e-05
LPIN2 [NCBI] 1.47454e-05
MMP2 [NCBI] 8.32127e-06



OMIM


 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



Database Center for Life Science