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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hyperostosis [NCBI]

Gene


 Gene Link Information
Gain		 01
SOST [NCBI] 7.16457e-05
FGF23 [NCBI] 2.77713e-05
FGFR3 [NCBI] 1.50307e-05
CTSH [NCBI] 1.25575e-05
COL6A1 [NCBI] 1.12037e-05
ANKH [NCBI] 1.05822e-05
ALPL [NCBI] 9.741e-06
PHEX [NCBI] 8.91372e-06
CTSL1 [NCBI] 6.22332e-06
ACP5 [NCBI] 5.90767e-06
STAT1 [NCBI] 5.83924e-06
TNFRSF11B [NCBI] 5.49173e-06
TGFB1 [NCBI] 3.85559e-06
CDKN1A [NCBI] 3.01271e-06



OMIM


 OMIM Link Information
gain		 01
proteus syndrome [NCBI] 0.00215012
IH [NCBI] 0.000697531
HHS [NCBI] 0.000573952
SRS [NCBI] 0.000328832
CDD [NCBI] 0.00022125
lenz-majewski hyperostotic dwarfism [NCBI] 0.000194697
SOST [NCBI] 0.000170451
ectodermal dysplasia with natal teeth, turnpenny type [NCBI] 0.000137445
hyperostosis cranialis interna [NCBI] 0.000137445
BMND1 [NCBI] 9.36381e-05
FGFR3 [NCBI] 8.68024e-05
hyperostosis corticalis generalisata [NCBI] 8.16836e-05
CMDD [NCBI] 7.23386e-05
GALNT3 [NCBI] 6.83464e-05
SOST [NCBI] 6.724e-05
MMP13 [NCBI] 6.724e-05
ANKH [NCBI] 6.724e-05
CRMO [NCBI] 5.39002e-05
FGF23 [NCBI] 5.08431e-05
TD1 [NCBI] 5.07618e-05
ACH [NCBI] 4.39526e-05
BGLAP [NCBI] 4.18653e-05
PTHLH [NCBI] 2.7952e-05
APC [NCBI] 1.06392e-05
VEGF [NCBI] 3.92706e-06



Database Center for Life Science