Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Musculoskeletal Abnormalities	[NCBI]

Gene	Link	Information Gain
ACRPV	[NCBI]	0.000438875
SBDSP	[NCBI]	0.000378131
SBDS	[NCBI]	4.81494e-05
GDF5	[NCBI]	2.08446e-05
SHOX	[NCBI]	1.7929e-05
SLC35A3	[NCBI]	1.53531e-05
TPST1	[NCBI]	1.44547e-05
PHF6	[NCBI]	1.21519e-05
LECT1	[NCBI]	1.09169e-05
HOXA1	[NCBI]	1.07494e-05
RAI1	[NCBI]	1.06713e-05
PAX1	[NCBI]	1.05967e-05
LRP6	[NCBI]	1.05967e-05
ACVR1	[NCBI]	9.54036e-06
AAAS	[NCBI]	9.35379e-06
PAX9	[NCBI]	9.25089e-06
ATRX	[NCBI]	8.91907e-06
IRF6	[NCBI]	8.76199e-06
CBX4	[NCBI]	8.71268e-06
FBN1	[NCBI]	7.76681e-06
RUNX2	[NCBI]	7.71186e-06
COL2A1	[NCBI]	7.34807e-06
FGFR2	[NCBI]	6.99454e-06
LMNA	[NCBI]	6.49196e-06
TGFBR1	[NCBI]	5.84828e-06
FGFR3	[NCBI]	5.41177e-06
HRAS	[NCBI]	3.98171e-06
VEGFA	[NCBI]	2.74257e-06

OMIM	Link	Information gain
acropectorovertebral dysplasia, f-form of	[NCBI]	0.00098052
spondyloepimetaphyseal dysplasia, sponastrime type	[NCBI]	0.000705355
marden-walker syndrome	[NCBI]	0.000592366
cayler cardiofacial syndrome	[NCBI]	0.000560268
SDS	[NCBI]	0.000469552
kabuki syndrome	[NCBI]	0.000419129
SBDS	[NCBI]	0.000153469
uruguay faciocardiomusculoskeletal syndrome	[NCBI]	0.00013578
microcephaly with chemotactic defect and transient hypogammaglobulinemia	[NCBI]	9.93282e-05
retinitis pigmentosa-deafness syndrome	[NCBI]	9.93282e-05
roifman syndrome	[NCBI]	9.93282e-05
SLC35A3	[NCBI]	9.30442e-05
KCS	[NCBI]	8.14952e-05
oculocerebrocutaneous syndrome	[NCBI]	8.00231e-05
TPST1	[NCBI]	7.92643e-05
COFS1	[NCBI]	7.51966e-05
MTTS2	[NCBI]	7.40637e-05
BFLS	[NCBI]	7.14886e-05
FST	[NCBI]	6.81758e-05
MADA	[NCBI]	6.7161e-05
MRXHF1	[NCBI]	6.7161e-05
ATRX	[NCBI]	6.53687e-05
SCDO1	[NCBI]	6.32541e-05
HCH	[NCBI]	6.22932e-05
LWD	[NCBI]	5.7498e-05
GJA5	[NCBI]	5.72439e-05
IRF6	[NCBI]	5.52508e-05
HOS	[NCBI]	5.32824e-05
CCD	[NCBI]	4.79537e-05
ATRX	[NCBI]	4.65908e-05
SMS	[NCBI]	4.44322e-05
BBS	[NCBI]	4.1442e-05
LMNA	[NCBI]	3.79646e-05
FBN1	[NCBI]	3.66028e-05
FGFR2	[NCBI]	3.44887e-05
SDC2	[NCBI]	3.345e-05