Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Elbow Joint [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 8.69867e-05
MB [NCBI] 3.39884e-05
PLOD2 [NCBI] 7.47986e-06
PRG4 [NCBI] 6.67661e-06
SS18 [NCBI] 6.46951e-06
L1CAM [NCBI] 5.95464e-06
GDF5 [NCBI] 5.9109e-06
F8 [NCBI] 5.51793e-06
MMP3 [NCBI] 5.41512e-06
FGFR2 [NCBI] 5.28123e-06
PMP22 [NCBI] 4.57909e-06
MMP13 [NCBI] 4.52434e-06
CTGF [NCBI] 3.7376e-06
IL1RN [NCBI] 3.41635e-06
MPO [NCBI] 2.67064e-06
TNF [NCBI] 1.37783e-06



OMIM


 OMIM Link Information
gain		 01
radial heads, posterior dislocation of [NCBI] 0.00300245
pterygium, antecubital [NCBI] 0.00117647
SEMDJL [NCBI] 0.00105937
bruck syndrome 1 [NCBI] 0.000983418
larsen syndrome, recessive [NCBI] 0.000844839
OFD4 [NCBI] 0.000844839
AMCN [NCBI] 0.000785125
RA [NCBI] 0.00077286
OD [NCBI] 0.000580475
LRS1 [NCBI] 0.000228229
HFTC [NCBI] 0.000218548
MB [NCBI] 0.00020195
megaepiphyseal dwarfism [NCBI] 0.000200836
mental retardation syndrome, mietens-weber type [NCBI] 0.000161582
BDB2 [NCBI] 0.000161582
HHS [NCBI] 0.000146781
corpus callosum, partial agenesis of, x-linked [NCBI] 0.000137177
radioulnar synostosis [NCBI] 0.000119639
noonan-like/multiple giant cell lesion syndrome [NCBI] 0.000119639
SYNS1 [NCBI] 0.000106127
CACP [NCBI] 9.70709e-05
ABS [NCBI] 9.18113e-05
AMC [NCBI] 6.85723e-05
PRG4 [NCBI] 4.02452e-05
L1CAM [NCBI] 3.79854e-05
FGFR2 [NCBI] 3.22061e-05
FMF [NCBI] 2.78454e-05
MUC1 [NCBI] 2.15579e-05
SLE [NCBI] 1.51513e-05
MPO [NCBI] 9.89579e-06
TNF [NCBI] 2.56091e-06



Database Center for Life Science