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MeSH keywords -> Related genes, diseases (OMIM)


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01 Dislocations [NCBI]

Gene


 Gene Link Information
Gain		 01
LRSL [NCBI] 0.000499621
HAPLN1 [NCBI] 2.06264e-05
NOS2 [NCBI] 1.6412e-05
CHST3 [NCBI] 1.45844e-05
PTGS1 [NCBI] 1.20245e-05
IL11 [NCBI] 1.03361e-05
RECQL4 [NCBI] 9.8353e-06
L1CAM [NCBI] 9.13281e-06
TNC [NCBI] 9.10424e-06
TNF [NCBI] 8.19693e-06
FGFR1 [NCBI] 7.95279e-06
TRPV1 [NCBI] 7.85459e-06
FGF2 [NCBI] 7.38155e-06
FLT1 [NCBI] 6.56865e-06
PTGS2 [NCBI] 6.46478e-06
MATN1 [NCBI] 6.41595e-06
CXCL1 [NCBI] 6.40432e-06
TNFSF11 [NCBI] 4.79991e-06
TNFRSF11B [NCBI] 4.75834e-06
CXCL12 [NCBI] 4.67208e-06
IL6 [NCBI] 3.90213e-06
MTHFR [NCBI] 3.88067e-06
CD68 [NCBI] 3.77047e-06
IL1RN [NCBI] 3.59574e-06
MPO [NCBI] 2.94313e-06
VEGFA [NCBI] 2.86216e-06
PCNA [NCBI] 2.71775e-06



OMIM


 OMIM Link Information
gain		 01
spondyloepimetaphyseal dysplasia with multiple dislocations [NCBI] 0.00290121
larsen syndrome, recessive [NCBI] 0.0022037
DBQD [NCBI] 0.00111324
patella, familial recurrent dislocation of [NCBI] 0.000975838
larsen-like syndrome [NCBI] 0.000975838
LRS1 [NCBI] 0.000973977
joint laxity, familial [NCBI] 0.000758187
scholte syndrome [NCBI] 0.000758187
radial heads, posterior dislocation of [NCBI] 0.000758187
kabuki syndrome [NCBI] 0.000630678
RA [NCBI] 0.000578049
OFD4 [NCBI] 0.000452068
microcephalic osteodysplastic primordial dwarfism, type i [NCBI] 0.000382824
pena-shokeir syndrome, type i [NCBI] 0.000252679
larsen-like syndrome, lethal type [NCBI] 0.000196473
pseudodiastrophic dysplasia [NCBI] 0.000159597
microspherophakia with hernia [NCBI] 0.000113606
megarbane syndrome [NCBI] 0.000113606
dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation [NCBI] 0.000113606
mental retardation, short stature, facial anomalies, and joint dislocations [NCBI] 0.000113606
mucopolysaccharidosis type iva [NCBI] 9.92366e-05
LWD [NCBI] 9.39864e-05
mental retardation syndrome, mietens-weber type [NCBI] 9.11475e-05
humeroradial synostosis [NCBI] 8.26799e-05
corpus callosum, partial agenesis of, x-linked [NCBI] 8.26799e-05
AMC [NCBI] 8.16296e-05
SLE [NCBI] 8.07809e-05
NF1 [NCBI] 6.30445e-05
catel-manzke syndrome [NCBI] 6.28292e-05
pneumothorax, primary spontaneous [NCBI] 5.79685e-05
three m syndrome [NCBI] 5.66306e-05
L1CAM [NCBI] 4.56347e-05
SEDC [NCBI] 3.96058e-05
VEGF [NCBI] 3.63748e-05
RTS [NCBI] 3.30892e-05
RSTS [NCBI] 3.15126e-05
hurler syndrome [NCBI] 3.05495e-05
LNS [NCBI] 3.03185e-05
TNF [NCBI] 2.22565e-05
TNFRSF11B [NCBI] 1.83597e-05
MPO [NCBI] 7.03632e-06
PCNA [NCBI] 5.87355e-06



Database Center for Life Science