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01 Epiphyses [NCBI]

Gene


 Gene Link Information
Gain		 01
ATD [NCBI] 0.000510938
PTH [NCBI] 1.92394e-05
TRPS1 [NCBI] 1.39361e-05
COL11A2 [NCBI] 1.11261e-05
HAPLN1 [NCBI] 9.72324e-06
BSX [NCBI] 9.20939e-06
MATN1 [NCBI] 8.82362e-06
SLC35D1 [NCBI] 7.72302e-06
ACP5 [NCBI] 6.91485e-06
COL9A2 [NCBI] 6.31537e-06
BHLHB2 [NCBI] 6.2783e-06
EIF2AK3 [NCBI] 6.24256e-06
EBP [NCBI] 6.20805e-06
PAX4 [NCBI] 5.81948e-06
ITGA1 [NCBI] 5.44119e-06
PCNA [NCBI] 4.84166e-06
PITX3 [NCBI] 4.75264e-06
COL2A1 [NCBI] 4.52763e-06
PITX1 [NCBI] 4.45485e-06
COMP [NCBI] 4.23072e-06
MGP [NCBI] 4.17627e-06
PTN [NCBI] 3.84223e-06
ATM [NCBI] 3.59809e-06
IBSP [NCBI] 3.32169e-06
XRCC5 [NCBI] 3.25894e-06
TNFRSF11B [NCBI] 3.00123e-06
CXCL12 [NCBI] 2.49367e-06
EGF [NCBI] 2.37361e-06
AR [NCBI] 1.86091e-06
TH [NCBI] 1.41866e-06
NPY [NCBI] 1.32153e-06



OMIM


 OMIM Link Information
gain		 01
epiphyseal dysplasia, microcephaly, and nystagmus [NCBI] 0.003449
metaphyseal acroscyphodysplasia [NCBI] 0.00278389
spondyloepiphyseal dysplasia tarda, autosomal dominant [NCBI] 0.00235593
osteoarthropathy of fingers, familial [NCBI] 0.00203025
trichoscyphodysplasia [NCBI] 0.00107278
SEMDJL [NCBI] 0.000955856
spondylometaphyseal dysplasia, kozlowski type [NCBI] 0.000955856
epiphyseal dysplasia, multiple, with early-onset diabetes mellitus [NCBI] 0.000804332
PSACH [NCBI] 0.000754549
hypertension with brachydactyly [NCBI] 0.000710324
EDM1 [NCBI] 0.000546258
OD [NCBI] 0.00048029
renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia [NCBI] 0.00047583
ATD1 [NCBI] 0.000405938
TRPS2 [NCBI] 0.00039517
fitzsimmons-guilbert syndrome [NCBI] 0.000380274
TRPS1 [NCBI] 0.000319445
RCDP1 [NCBI] 0.00028999
OSMED [NCBI] 0.000272206
spondyloepimetaphyseal dysplasia, strudwick type [NCBI] 0.000238769
multiple epiphyseal dysplasia with robin phenotype [NCBI] 0.000189909
ASPED [NCBI] 0.000189909
symphalangism of toes [NCBI] 0.000189909
epiphyseal dysplasia of femoral head, myopia, and deafness [NCBI] 0.000189909
macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance [NCBI] 0.000189909
spondyloepimetaphyseal dysplasia, micromelic [NCBI] 0.000189909
megaepiphyseal dwarfism [NCBI] 0.000189909
satoyoshi syndrome [NCBI] 0.000189909
SRS [NCBI] 0.000185453
RA [NCBI] 0.000173963
morquio syndrome, nonkeratosulfate-excreting type [NCBI] 0.000150666
ACFD [NCBI] 0.000150666
growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction [NCBI] 0.000150666
puerto rican infant hypotonia syndrome [NCBI] 0.000150666
lissencephaly type iii and bone dysplasia [NCBI] 0.000135876
legg-calve-perthes disease [NCBI] 0.000126283
EDM4 [NCBI] 0.000119159
hunter-mcalpine craniosynostosis syndrome [NCBI] 0.000119159
schneckenbecken dysplasia [NCBI] 0.000119159
EIF2AK3 [NCBI] 8.9295e-05
SLSN1 [NCBI] 8.27066e-05
PPAC [NCBI] 8.27066e-05
mucopolysaccharidosis type vi [NCBI] 7.53781e-05
mucopolysaccharidosis type vii [NCBI] 7.41243e-05
ehlers-danlos syndrome, type iv, autosomal dominant [NCBI] 7.41243e-05
EVC [NCBI] 7.06812e-05
PTH [NCBI] 6.52067e-05
osteogenesis imperfecta, type iia [NCBI] 6.40499e-05
CRMO [NCBI] 5.87648e-05
brain-specific homeobox, mouse, homolog of [NCBI] 5.33205e-05
SDS [NCBI] 5.2184e-05
CHH [NCBI] 5.1663e-05
AHO [NCBI] 5.11526e-05
DSPG3 [NCBI] 4.95533e-05
SLC35D1 [NCBI] 4.95533e-05
ACH [NCBI] 4.45505e-05
COL9A2 [NCBI] 4.38397e-05
BHLHB2 [NCBI] 4.26348e-05
TRPS1 [NCBI] 4.16036e-05
PAX4 [NCBI] 4.07021e-05
MATN3 [NCBI] 3.99013e-05
PAPSS2 [NCBI] 3.9181e-05
COL11A2 [NCBI] 3.85265e-05
mucopolysaccharidosis type iva [NCBI] 3.28048e-05
AIS [NCBI] 3.14173e-05
COMP [NCBI] 1.79704e-05
PCNA [NCBI] 1.1776e-05
ACP5 [NCBI] 1.07406e-05
TNFRSF11B [NCBI] 9.60055e-06
SPP1 [NCBI] 8.35811e-06
VEGF [NCBI] 6.93344e-06
PWS [NCBI] 4.77234e-06
AR [NCBI] 3.29758e-06
AVP [NCBI] 1.53669e-06
TH [NCBI] 8.28203e-07
NPY [NCBI] 5.33436e-07
EGF [NCBI] 4.28196e-07



Database Center for Life Science