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MeSH keywords -> Related genes, diseases (OMIM)


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01 Scapula [NCBI]

Gene


 Gene Link Information
Gain		 01
PAX1 [NCBI] 4.56523e-05
COMP [NCBI] 1.13773e-05
LOC441056 [NCBI] 9.94557e-06
LOC653543 [NCBI] 9.94557e-06
LOC653548 [NCBI] 9.94557e-06
LOC653541 [NCBI] 9.94557e-06
LOC728410 [NCBI] 9.94557e-06
LOC653544 [NCBI] 9.94557e-06
LOC653545 [NCBI] 9.94557e-06
DUX4 [NCBI] 8.3156e-06
CPZ [NCBI] 8.07864e-06
CD68 [NCBI] 7.56503e-06
HOXC8 [NCBI] 6.84691e-06
TTF1 [NCBI] 6.75853e-06
EYA1 [NCBI] 6.42579e-06
CDX1 [NCBI] 6.10072e-06
PTH1R [NCBI] 5.90261e-06
ACVRL1 [NCBI] 5.84444e-06
WNT4 [NCBI] 5.21854e-06
PAX3 [NCBI] 4.983e-06
HAPLN1 [NCBI] 4.88759e-06
MATN1 [NCBI] 4.43853e-06
NOG [NCBI] 3.94819e-06
PTEN [NCBI] 3.36354e-06
LPL [NCBI] 2.95849e-06



OMIM


 OMIM Link Information
gain		 01
amyotrophy, neurogenic scapuloperoneal, new england type [NCBI] 0.00334884
sprengel deformity [NCBI] 0.00334884
acromial dimples [NCBI] 0.00196614
pierre robin sequence with pectus excavatum and rib and scapular anomalies [NCBI] 0.00196614
nevus flammeus of nape of neck [NCBI] 0.00104185
scapuloperoneal syndrome, neurogenic, kaeser type [NCBI] 0.000901645
pelvis-shoulder dysplasia [NCBI] 0.000859142
klippel-feil syndrome, autosomal recessive [NCBI] 0.000849287
klippel-feil syndrome, autosomal dominant [NCBI] 0.000748482
spondyloenchondrodysplasia [NCBI] 0.000711442
SPMM [NCBI] 0.000507315
proteus syndrome [NCBI] 0.000460917
poland syndrome [NCBI] 0.000377037
syndesmodysplasic dwarfism [NCBI] 0.000213171
scapuloperoneal myopathy, x-linked dominant [NCBI] 0.000213171
costocoracoid ligament, congenitally short [NCBI] 0.000213171
pelviscapular dysplasia [NCBI] 0.000213171
superior transverse scapular ligament, calcification of, familial [NCBI] 0.000213171
FSHMD1A [NCBI] 0.000185728
hydrocephalus, skeletal anomalies, and mental disturbance [NCBI] 0.000173908
d-2-@hydroxyglutaric aciduria [NCBI] 0.000142342
EDMD2 [NCBI] 0.000109289
PPAC [NCBI] 0.000105656
amyloidosis, primary cutaneous [NCBI] 0.000104004
HNA [NCBI] 0.000100967
HFTC [NCBI] 0.000100967
exostoses, multiple, type i [NCBI] 9.95651e-05
SCDO1 [NCBI] 8.58441e-05
RDT [NCBI] 7.79642e-05
EDMD [NCBI] 7.67486e-05
COMP [NCBI] 6.90398e-05
CPZ [NCBI] 5.37697e-05
FHL1 [NCBI] 5.37697e-05
SOX9 [NCBI] 4.09589e-05
MUC1 [NCBI] 2.3461e-05
RA [NCBI] 1.80622e-05
SLE [NCBI] 1.67696e-05
LPL [NCBI] 1.45439e-05



Database Center for Life Science