Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Leg Bones [NCBI]

Gene


 Gene Link Information
Gain		 01
ACP5 [NCBI] 1.0182e-05
TRIM37 [NCBI] 8.43715e-06
COL10A1 [NCBI] 8.25995e-06
PLCB1 [NCBI] 6.97894e-06
PITX3 [NCBI] 6.33533e-06
PITX1 [NCBI] 6.03665e-06
MMP13 [NCBI] 5.24974e-06
BMP7 [NCBI] 4.96998e-06
CTSL1 [NCBI] 4.31155e-06



OMIM


 OMIM Link Information
gain		 01
cranioectodermal dysplasia [NCBI] 0.0015153
spondyloepimetaphyseal dysplasia, strudwick type [NCBI] 0.000577465
spondyloepimetaphyseal dysplasia, type ii [NCBI] 0.000192358
MCDS [NCBI] 0.00016988
osteoporosis, juvenile [NCBI] 0.00016514
camurati-engelmann disease [NCBI] 0.000142421
mulibrey nanism [NCBI] 0.000142421
MMP13 [NCBI] 5.06425e-05
COL10A1 [NCBI] 5.06425e-05
GLI3 [NCBI] 4.65775e-05
ACP5 [NCBI] 2.39806e-05
SPP1 [NCBI] 2.13476e-05
SHH [NCBI] 2.10187e-05
RA [NCBI] 8.97234e-07
SLE [NCBI] 8.37634e-07



Database Center for Life Science