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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hyperostosis, Cortical, Congenital [NCBI]

Gene


 Gene Link Information
Gain		 01
COL1A1 [NCBI] 2.49851e-05
CD79A [NCBI] 1.1821e-05



OMIM


 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



Database Center for Life Science