Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Elbow Joint	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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