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MeSH keywords -> Related genes, diseases (OMIM)


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01 Joint Instability [NCBI]

Gene


 Gene Link Information
Gain		 01
DBQD [NCBI] 0.000355204
MS [NCBI] 3.75925e-05
TNXB [NCBI] 3.5386e-05
BMP2 [NCBI] 3.27313e-05
MATN1 [NCBI] 1.60354e-05
GOLGA6B [NCBI] 1.49592e-05
GOLGA6 [NCBI] 1.49592e-05
PEPD [NCBI] 1.14212e-05
LOX [NCBI] 9.72169e-06
PITX1 [NCBI] 9.47847e-06
ADAMTS2 [NCBI] 9.12159e-06
COL1A2 [NCBI] 8.75071e-06
SOX9 [NCBI] 7.99874e-06
COL2A1 [NCBI] 7.85035e-06
CHI3L1 [NCBI] 7.66414e-06
PTGES2 [NCBI] 7.4963e-06
BMP4 [NCBI] 7.2184e-06
BAK1 [NCBI] 6.97309e-06
MMP13 [NCBI] 6.65835e-06
KRAS [NCBI] 6.04681e-06
PTGS1 [NCBI] 5.1737e-06
PTEN [NCBI] 4.05601e-06
CTNNB1 [NCBI] 3.6291e-06
PTGS2 [NCBI] 2.44777e-06



OMIM


 OMIM Link Information
gain		 01
SEMDJL [NCBI] 0.00676933
ehlers-danlos syndrome, type vib [NCBI] 0.00108048
DBQD [NCBI] 0.00105078
patella, familial recurrent dislocation of [NCBI] 0.000945056
cutis laxa, corneal clouding, and mental retardation [NCBI] 0.000521908
larsen syndrome, recessive [NCBI] 0.000495958
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth [NCBI] 0.000454472
PAND1 [NCBI] 0.000454472
GO [NCBI] 0.000454472
ehlers-danlos syndrome, type viii [NCBI] 0.000437344
spondyloepimetaphyseal dysplasia with multiple dislocations [NCBI] 0.000437344
ehlers-danlos syndrome, type iii [NCBI] 0.000389149
OD [NCBI] 0.000306636
coffin-siris syndrome [NCBI] 0.00028242
spondylometaphyseal dysplasia with dentinogenesis imperfecta [NCBI] 0.00021303
kabuki syndrome [NCBI] 0.000182192
costello syndrome [NCBI] 0.000179087
short syndrome [NCBI] 0.000171102
COL1A2 [NCBI] 0.000167799
RA [NCBI] 0.000142733
megarbane syndrome [NCBI] 0.00012182
spondyloepiphyseal dysplasia with atlantoaxial instability [NCBI] 0.00012182
mental retardation, short stature, facial anomalies, and joint dislocations [NCBI] 0.00012182
hydrocephalus, tall stature, joint laxity, and kyphoscoliosis [NCBI] 0.00012182
SEDC [NCBI] 0.00011815
spondyloepimetaphyseal dysplasia, shohat type [NCBI] 9.93556e-05
cerebrofacioarticular syndrome [NCBI] 9.93556e-05
LUM [NCBI] 7.79e-05
PITX1 [NCBI] 7.45227e-05
FMOD [NCBI] 6.83464e-05
TNXB [NCBI] 6.26709e-05
COL11A1 [NCBI] 6.10772e-05
COL11A2 [NCBI] 6.10772e-05
cutis laxa, autosomal recessive, type i [NCBI] 5.68226e-05
UCMD [NCBI] 5.46345e-05
cutis laxa, x-linked [NCBI] 5.39676e-05
BMP4 [NCBI] 5.26625e-05
STL1 [NCBI] 4.67624e-05
NPS [NCBI] 3.76845e-05
ACP5 [NCBI] 2.79341e-05
BWS [NCBI] 1.5133e-05
CD [NCBI] 5.9763e-06
VEGF [NCBI] 2.33609e-06
SLE [NCBI] 1.30453e-06



Database Center for Life Science