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MeSH keywords -> Related genes, diseases (OMIM)


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01 Cleidocranial Dysplasia [NCBI]


Gene


Gene Link Information
Gain
01
RUNX2 [NCBI] 0.000449004
RUNX1 [NCBI] 3.6789e-05
SMAD3 [NCBI] 1.39632e-05
OSTF1 [NCBI] 1.269e-05
MSX2 [NCBI] 1.02603e-05
ALX4 [NCBI] 1.017e-05
VEGFB [NCBI] 9.70974e-06
SMAD1 [NCBI] 8.37678e-06
BMP6 [NCBI] 8.09315e-06
EDA [NCBI] 7.3441e-06
FGF4 [NCBI] 7.29434e-06
RUNX3 [NCBI] 7.19898e-06
SHOX [NCBI] 6.99534e-06
IBSP [NCBI] 6.20066e-06
CKAP4 [NCBI] 5.60791e-06
TP63 [NCBI] 4.88732e-06
BMP2 [NCBI] 4.45522e-06
LIF [NCBI] 4.15596e-06
VEGFA [NCBI] 2.07063e-06




OMIM


OMIM Link Information
gain
01
CCD [NCBI] 0.00966752
cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia [NCBI] 0.00423007
RUNX2 [NCBI] 0.00123849
acrodysostosis [NCBI] 0.000705355
pycnodysostosis [NCBI] 0.000125063
hypophosphatasia, adult type [NCBI] 0.000123223
cleidocranial dysplasia, recessive form [NCBI] 0.000113208
PFMCCD [NCBI] 0.000113208
hypophosphatasia, infantile [NCBI] 0.000101003
VEGFB [NCBI] 6.6266e-05
ALX4 [NCBI] 6.00921e-05
CBFB [NCBI] 6.00921e-05
MSX2 [NCBI] 5.53239e-05
PFM [NCBI] 5.386e-05
crouzon syndrome [NCBI] 4.91306e-05
TCOF1 [NCBI] 4.82111e-05
BMP2 [NCBI] 4.69163e-05
ALPL [NCBI] 4.65199e-05
aspartylglucosaminuria [NCBI] 4.47463e-05
andersen cardiodysrhythmic periodic paralysis [NCBI] 4.31125e-05
RUNX1 [NCBI] 4.21875e-05
ODDD [NCBI] 3.96565e-05
exostoses, multiple, type i [NCBI] 3.79854e-05
WS1 [NCBI] 3.13879e-05
TCOF [NCBI] 2.99447e-05
HGPS [NCBI] 2.80216e-05
ACH [NCBI] 2.1116e-05
BCNS [NCBI] 1.62379e-05
MFS [NCBI] 1.115e-05




Database Center for Life Science