Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Cleidocranial Dysplasia	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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