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01 Osteochondrodysplasias [NCBI]

Gene


 Gene Link Information
Gain		 01
RMRP [NCBI] 0.00251437
DBQD [NCBI] 0.000686903
COL2A1 [NCBI] 0.000524849
MATN1 [NCBI] 0.000490066
SHOX [NCBI] 0.00048948
FGFR3 [NCBI] 0.000406934
SLC26A2 [NCBI] 0.000394957
COMP [NCBI] 0.000388155
MMEDF [NCBI] 0.000341765
SEDLP7 [NCBI] 0.000341765
SEDLP2 [NCBI] 0.000341765
SEDLP5 [NCBI] 0.000341765
CMDR [NCBI] 0.000341765
SEDLP3 [NCBI] 0.000341765
SEDLP4 [NCBI] 0.000341765
SEDLP6 [NCBI] 0.000341765
TRAPPC2 [NCBI] 0.000335256
SOX9 [NCBI] 0.000325324
ATD [NCBI] 0.000281036
COL10A1 [NCBI] 0.000176011
SMARCAL1 [NCBI] 0.000134555
MATN3 [NCBI] 9.99549e-05
COL9A2 [NCBI] 9.71635e-05
WISP3 [NCBI] 9.31374e-05
SBDS [NCBI] 7.69856e-05
COL9A3 [NCBI] 7.65408e-05
PTH1R [NCBI] 7.29736e-05
DYM [NCBI] 6.40366e-05
TRPS1 [NCBI] 6.28828e-05
COL11A2 [NCBI] 5.49764e-05
GDF5 [NCBI] 3.56377e-05
HSPG2 [NCBI] 3.31201e-05
SOST [NCBI] 3.16543e-05
ACAN [NCBI] 3.06736e-05
PTHLH [NCBI] 3.02387e-05
COL9A1 [NCBI] 2.80241e-05
TYROBP [NCBI] 2.79003e-05
PTH [NCBI] 2.71735e-05
FLNB [NCBI] 2.64575e-05
PAPSS1 [NCBI] 2.56677e-05
EIF2AK3 [NCBI] 2.52609e-05
SRY [NCBI] 2.44069e-05
PAPSS2 [NCBI] 2.23896e-05
CHST3 [NCBI] 2.23896e-05
FLNA [NCBI] 1.93916e-05
HAPLN1 [NCBI] 1.79379e-05
COL11A1 [NCBI] 1.582e-05
ARSE [NCBI] 1.53296e-05
FGF3 [NCBI] 1.4282e-05
TREM2 [NCBI] 1.41787e-05
C9orf128 [NCBI] 1.2832e-05
CTSK [NCBI] 1.24371e-05
SLC26A3 [NCBI] 1.24371e-05
CHST1 [NCBI] 1.04525e-05
MATN4 [NCBI] 1.04525e-05
FGF23 [NCBI] 1.03724e-05
RPS19 [NCBI] 9.85823e-06
LIFR [NCBI] 9.81372e-06
YKT6 [NCBI] 8.97247e-06
CRTAP [NCBI] 8.97247e-06
EVC2 [NCBI] 7.90822e-06
COLQ [NCBI] 7.44881e-06
VCX [NCBI] 7.25859e-06
TLN1 [NCBI] 7.25859e-06
NPR2 [NCBI] 7.08756e-06
DLL3 [NCBI] 6.53689e-06
FRS2 [NCBI] 6.42331e-06
RPP14 [NCBI] 6.31689e-06
THBS2 [NCBI] 6.31689e-06
PAX1 [NCBI] 5.71632e-06
BMP3 [NCBI] 5.64573e-06
BGLAP [NCBI] 5.51291e-06
MEPE [NCBI] 5.45027e-06
RAD54L [NCBI] 5.45027e-06
WISP1 [NCBI] 5.45027e-06
NCAN [NCBI] 5.45027e-06
SOX3 [NCBI] 5.27538e-06
SFRP4 [NCBI] 5.11719e-06
IL11RA [NCBI] 4.97283e-06
EXT1 [NCBI] 4.88317e-06
PAX9 [NCBI] 4.39627e-06
NOV [NCBI] 4.33279e-06
CDC42 [NCBI] 4.33279e-06
ATRX [NCBI] 4.07457e-06
ALPL [NCBI] 4.02243e-06
DIO2 [NCBI] 3.89909e-06
SOX10 [NCBI] 3.76275e-06
TNNT2 [NCBI] 3.678e-06
DKC1 [NCBI] 3.65751e-06
GLI3 [NCBI] 3.57814e-06
MIA [NCBI] 3.4843e-06
AIRE [NCBI] 3.34509e-06
ACP5 [NCBI] 3.19471e-06
TREM1 [NCBI] 3.14284e-06
RUNX2 [NCBI] 2.92624e-06
VCAN [NCBI] 2.63062e-06
GRB2 [NCBI] 2.0368e-06
FXN [NCBI] 1.78875e-06
MMP13 [NCBI] 1.54572e-06
GAPDH [NCBI] 1.39474e-06
TGFBR1 [NCBI] 1.29365e-06
IGF1 [NCBI] 1.04165e-06
EGF [NCBI] 9.7213e-07
BMP2 [NCBI] 7.97672e-07
CTGF [NCBI] 6.95548e-07
STAT1 [NCBI] 6.56228e-07
CDKN1A [NCBI] 5.03492e-07
TNFSF11 [NCBI] 4.68548e-07



OMIM


 OMIM Link Information
gain		 01
SEMDJL [NCBI] 0.00532626
ATD1 [NCBI] 0.00524894
hypertrichotic osteochondrodysplasia [NCBI] 0.0033799
spondyloenchondrodysplasia [NCBI] 0.00336962
spondyloepimetaphyseal dysplasia with multiple dislocations [NCBI] 0.00303313
spondyloepiphyseal dysplasia tarda, autosomal dominant [NCBI] 0.00274505
PSACH [NCBI] 0.00251136
LWD [NCBI] 0.00238414
spondylometaphyseal dysplasia, sedaghatian type [NCBI] 0.00232563
fibrochondrogenesis [NCBI] 0.00212063
SJS1 [NCBI] 0.00211147
macrocephaly with multiple epiphyseal dysplasia and distinctive facies [NCBI] 0.00203579
SEDC [NCBI] 0.00189713
CHH [NCBI] 0.00186655
dyssegmental dysplasia, rolland-desbuquois type [NCBI] 0.00185339
apnea, obstructive sleep [NCBI] 0.00178906
omodysplasia, generalized form [NCBI] 0.00175523
COMP [NCBI] 0.00160187
opsismodysplasia [NCBI] 0.0015109
COL2A1 [NCBI] 0.00137192
spondylometaphyseal dysplasia, type a4 [NCBI] 0.00135593
PPAC [NCBI] 0.00119823
immunoosseous dysplasia, schimke type [NCBI] 0.00119432
COL10A1 [NCBI] 0.00115802
spondyloepimetaphyseal dysplasia, sponastrime type [NCBI] 0.00114764
TD1 [NCBI] 0.00107641
spondylometaphyseal dysplasia, corner fracture type [NCBI] 0.0010578
kyphomelic dysplasia [NCBI] 0.00103911
SLE [NCBI] 0.00103707
FGFR3 [NCBI] 0.00100234
microcephalic osteodysplastic primordial dwarfism, type ii [NCBI] 0.000993635
MCDS [NCBI] 0.000984868
HCH [NCBI] 0.000939004
spondylometaphyseal dysplasia, kozlowski type [NCBI] 0.000924218
GHDD [NCBI] 0.000924218
omodysplasia [NCBI] 0.000924218
ACG1A [NCBI] 0.000880727
TRAPPC2 [NCBI] 0.00087445
SEDT [NCBI] 0.000822139
microcephalic osteodysplastic primordial dwarfism, type i [NCBI] 0.000819511
stuve-wiedemann syndrome [NCBI] 0.000771795
epiphyseal dysplasia, microcephaly, and nystagmus [NCBI] 0.000763894
SOX9 [NCBI] 0.000745203
EDM1 [NCBI] 0.000718107
diastrophic dysplasia [NCBI] 0.000706001
leukoencephalopathy with metaphyseal chondrodysplasia [NCBI] 0.000677333
spondyloepiphyseal dysplasia-brachydactyly and distinctive speech [NCBI] 0.000677333
upington disease [NCBI] 0.000677333
epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia [NCBI] 0.000677333
metaphyseal dysplasia, braun-tinschert type [NCBI] 0.000677333
czech dysplasia, metatarsal type [NCBI] 0.000677333
epiphyseal dysplasia, multiple, with miniepiphyses [NCBI] 0.000677333
SLC26A2 [NCBI] 0.000674526
campomelic dysplasia [NCBI] 0.000654422
enchondromatosis, multiple [NCBI] 0.000643294
GO [NCBI] 0.00062112
langer mesomelic dysplasia [NCBI] 0.000598822
BOCD [NCBI] 0.000582291
MNS [NCBI] 0.000575323
short rib-polydactyly syndrome, type iii [NCBI] 0.000554869
DBQD [NCBI] 0.000526915
SHOX [NCBI] 0.000517793
spondyloepimetaphyseal dysplasia, strudwick type [NCBI] 0.000463737
OSMED [NCBI] 0.000463713
synostosis, carpal, with dysplastic elbow joints and brachydactyly [NCBI] 0.000461495
acromicric dysplasia [NCBI] 0.000461495
spondyloepiphyseal dysplasia tarda, autosomal recessive [NCBI] 0.000461495
short rib-polydactyly syndrome, type ii [NCBI] 0.000437616
ACH [NCBI] 0.000419984
EDM3 [NCBI] 0.000414284
kniest dysplasia [NCBI] 0.000412981
EDM4 [NCBI] 0.000404658
hip dysplasia, beukes type [NCBI] 0.00038135
AOI [NCBI] 0.000362979
PTHR1 [NCBI] 0.000351364
ACG2 [NCBI] 0.000343025
EDM2 [NCBI] 0.000331367
oculodentoosseous dysplasia, recessive [NCBI] 0.000330048
nievergelt syndrome [NCBI] 0.000330048
MATN3 [NCBI] 0.000329204
metaphyseal chondrodysplasia, jansen type [NCBI] 0.000314449
AOII [NCBI] 0.000314449
RMRP [NCBI] 0.000307059
dermochondrocorneal dystrophy [NCBI] 0.000292444
COL9A3 [NCBI] 0.000284627
SDS [NCBI] 0.000278218
COL9A2 [NCBI] 0.000269889
SMC [NCBI] 0.000269653
microcephalic osteodysplastic primordial dwarfism, type iii [NCBI] 0.00026291
HSPG2 [NCBI] 0.000250097
DMC [NCBI] 0.000248509
spondylometaepiphyseal dysplasia, short limb-hand type [NCBI] 0.00024848
EDM5 [NCBI] 0.00024848
spondyloepiphyseal dysplasia, kimberley type [NCBI] 0.00024848
rhizomelic dysplasia, patterson-lowry type [NCBI] 0.00024848
spondyloepimetaphyseal dysplasia, type ii [NCBI] 0.00024848
CMDR [NCBI] 0.000238706
metatropic dwarfism [NCBI] 0.000238706
hodgkin disease, x-linked pseudoautosomal [NCBI] 0.000238706
RCDP1 [NCBI] 0.000234399
serpentine fibula-polycystic kidney syndrome [NCBI] 0.000231631
AMDM [NCBI] 0.000215168
spondylometaphyseal dysplasia, algerian type [NCBI] 0.000212115
DDSH [NCBI] 0.000212115
COL9A1 [NCBI] 0.000211186
WISP3 [NCBI] 0.000211186
geleophysic dysplasia [NCBI] 0.000185329
PLSDT [NCBI] 0.000181356
gonadal dysgenesis, xy type [NCBI] 0.000171705
spondyloepimetaphyseal dysplasia, x-linked [NCBI] 0.000165623
achondrogenesis, type iii [NCBI] 0.000165623
spondyloepimetaphyseal dysplasia with hypotrichosis [NCBI] 0.000165623
spondyloepimetaphyseal dysplasia, shohat type [NCBI] 0.000165623
achondrogenesis, type iv [NCBI] 0.000165623
boomerang dysplasia [NCBI] 0.000163175
acromesomelic dysplasia, hunter-thompson type [NCBI] 0.000156203
hydrops-ectopic calcification-moth-eaten skeletal dysplasia [NCBI] 0.000150141
blue rubber bleb nevus [NCBI] 0.000148524
short rib-polydactyly syndrome, type iv [NCBI] 0.000148524
epiphyseal dysplasia, multiple, with early-onset diabetes mellitus [NCBI] 0.000144778
acroosteolysis with osteoporosis and changes in skull and mandible [NCBI] 0.000138543
mohr syndrome [NCBI] 0.000138543
OSCS [NCBI] 0.000138543
GDF5 [NCBI] 0.000136956
WZS [NCBI] 0.000135618
spondylometaphyseal dysplasia with dentinogenesis imperfecta [NCBI] 0.000134767
micromelic bone dysplasia with cloverleaf skull [NCBI] 0.000134767
metaphyseal anadysplasia [NCBI] 0.000134767
osteoarthritis with mild chondrodysplasia [NCBI] 0.000134767
TRPS1 [NCBI] 0.000129948
varadi-papp syndrome [NCBI] 0.000129428
SMARCAL1 [NCBI] 0.000124485
OPD2 [NCBI] 0.000121431
roifman syndrome [NCBI] 0.000120874
gurrieri syndrome [NCBI] 0.000120874
COL11A2 [NCBI] 0.000114679
COL11A1 [NCBI] 0.000114679
PLOSL [NCBI] 0.000113098
SOST [NCBI] 0.000113098
spondyloperipheral dysplasia [NCBI] 0.000111368
TRPS1 [NCBI] 0.000106069
DYM [NCBI] 0.000105521
TRPS3 [NCBI] 0.000104106
STL2 [NCBI] 9.82258e-05
TD2 [NCBI] 9.32857e-05
chondrodysplasia, grebe type [NCBI] 8.529e-05
FLNB [NCBI] 8.29488e-05
EIF2AK3 [NCBI] 8.29488e-05
AGC1 [NCBI] 8.29488e-05
EVC2 [NCBI] 8.29488e-05
spondylometaphyseal dysplasia, axial [NCBI] 8.27967e-05
rhyns syndrome [NCBI] 8.27967e-05
ulna and fibula, hypoplasia of [NCBI] 8.27967e-05
osteosclerotic chondrodysplasia, lethal, with intracellular inclusions [NCBI] 8.27967e-05
spondyloepimetaphyseal dysplasia, matrilin-3 related [NCBI] 8.27967e-05
craniodiaphyseal dysplasia, dominant [NCBI] 8.27967e-05
spondyloepimetaphyseal dysplasia with abnormal dentition [NCBI] 8.27967e-05
chondrodysplasia calcificans metaphysealis [NCBI] 8.27967e-05
multiple epiphyseal dysplasia with robin phenotype [NCBI] 8.27967e-05
syndesmodysplasic dwarfism [NCBI] 8.27967e-05
osebold skeletal dysplasia/osteolysis syndrome [NCBI] 8.27967e-05
thoracic dysplasia-hydrocephalus syndrome [NCBI] 8.27967e-05
spondyloepiphyseal dysplasia with atlantoaxial instability [NCBI] 8.27967e-05
spondyloepiphyseal dysplasia tarda with characteristic facies [NCBI] 8.27967e-05
spondyloepiphyseal dysplasia, omani type [NCBI] 8.27967e-05
osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension [NCBI] 8.27967e-05
short stature syndrome, brussels type [NCBI] 8.27967e-05
spondyloepimetaphyseal dysplasia, x-linked, with mental deterioration [NCBI] 8.27967e-05
chondrodysplasia, lethal, with long bone angulation and mixed bone density [NCBI] 8.27967e-05
spondyloepiphyseal dysplasia, myopia, and sensorineural deafness [NCBI] 8.27967e-05
spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation [NCBI] 8.27967e-05
chondrodysplasia-pseudohermaphroditism syndrome [NCBI] 8.27967e-05
spondyloepimetaphyseal dysplasia, micromelic [NCBI] 8.27967e-05
spondyloepiphyseal dysplasia tarda with mental retardation [NCBI] 8.27967e-05
dyssegmental dysplasia with glaucoma [NCBI] 8.27967e-05
STL1 [NCBI] 8.05566e-05
frank-ter haar syndrome [NCBI] 7.98782e-05
PAPSS2 [NCBI] 7.98782e-05
hyperostosis corticalis generalisata [NCBI] 7.89581e-05
SOST [NCBI] 7.48926e-05
MMP13 [NCBI] 7.48926e-05
VEGF [NCBI] 7.1534e-05
OPD1 [NCBI] 7.14166e-05
LRS1 [NCBI] 6.92743e-05
chondrodysplasia punctata, autosomal dominant [NCBI] 6.92743e-05
marshall syndrome [NCBI] 6.92743e-05
pycnodysostosis [NCBI] 6.54073e-05
FMD [NCBI] 6.54073e-05
CHST3 [NCBI] 6.22245e-05
MEOX1 [NCBI] 6.22245e-05
COL19A1 [NCBI] 6.22245e-05
combined immunodeficiency with autoimmunity and spondylometaphyseal dysplasia [NCBI] 6.04223e-05
kniest-like dysplasia with pursed lips and ectopia lentis [NCBI] 6.04223e-05
thanatophoric dysplasia, glasgow variant [NCBI] 6.04223e-05
platyspondyly with amelogenesis imperfecta [NCBI] 6.04223e-05
second metatarsal-metacarpal syndrome [NCBI] 6.04223e-05
acrofrontofacionasal dysostosis syndrome [NCBI] 6.04223e-05
pyknoachondrogenesis [NCBI] 6.04223e-05
micromelic dysplasia, congenital, with dislocation of radius [NCBI] 6.04223e-05
spondylometaphyseal dysplasia, east african type [NCBI] 6.04223e-05
thoracopelvic dysostosis [NCBI] 6.04223e-05
metaphyseal dysplasia without hypotrichosis [NCBI] 6.04223e-05
anauxetic dysplasia [NCBI] 5.20385e-05
pacman dysplasia [NCBI] 5.20385e-05
codas syndrome [NCBI] 5.20385e-05
ASPED [NCBI] 5.20385e-05
osteogenesis imperfecta, type iib [NCBI] 5.20385e-05
EGF [NCBI] 5.15133e-05
FRNS [NCBI] 4.9642e-05
camurati-engelmann disease [NCBI] 4.9257e-05
TCL6 [NCBI] 4.84627e-05
TLN1 [NCBI] 4.84627e-05
CRTL1 [NCBI] 4.84627e-05
osteogenesis imperfecta, type vii [NCBI] 4.66284e-05
TLPD [NCBI] 4.66284e-05
ACG1B [NCBI] 4.66284e-05
satoyoshi syndrome [NCBI] 4.66284e-05
SCDO1 [NCBI] 4.63588e-05
PAPSS1 [NCBI] 4.32803e-05
CRTAP [NCBI] 4.32803e-05
IL11RA [NCBI] 4.32803e-05
OPTA1 [NCBI] 4.26308e-05
exostoses, multiple, type i [NCBI] 4.06303e-05
STL3 [NCBI] 3.9465e-05
weyers ulnar ray/oligodactyly syndrome [NCBI] 3.9465e-05
neuroblastoma stage 4s gene [NCBI] 3.74287e-05
LEPRE1 [NCBI] 3.74287e-05
MATN1 [NCBI] 3.74287e-05
BMPR1B [NCBI] 3.74287e-05
SBDS [NCBI] 3.74287e-05
pseudodiastrophic dysplasia [NCBI] 3.68489e-05
achondroplasia, so-called, and severe combined immunodeficiency [NCBI] 3.68489e-05
schneckenbecken dysplasia [NCBI] 3.68489e-05
PPIB [NCBI] 3.5446e-05
chondrodysplasia punctata, tibia-metacarpal type [NCBI] 3.46234e-05
CDC42 [NCBI] 3.38005e-05
TBCE [NCBI] 3.38005e-05
ITGB1 [NCBI] 3.23945e-05
RASSF1 [NCBI] 3.11677e-05
PTH [NCBI] 3.11608e-05
por deficiency [NCBI] 3.09835e-05
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus [NCBI] 3.09835e-05
JWS [NCBI] 2.9458e-05
d-2-@hydroxyglutaric aciduria [NCBI] 2.9458e-05
PABPN1 [NCBI] 2.91031e-05
BMPR1A [NCBI] 2.74068e-05
three m syndrome [NCBI] 2.68265e-05
LIFR [NCBI] 2.47218e-05
CTSK [NCBI] 2.41557e-05
GLI3 [NCBI] 2.13385e-05
CDPX1 [NCBI] 2.10587e-05
omenn syndrome [NCBI] 2.10587e-05
SPP1 [NCBI] 2.07636e-05
EPHX1 [NCBI] 1.98518e-05
CMDD [NCBI] 1.95909e-05
FLNA [NCBI] 1.7208e-05
contractural arachnodactyly, congenital [NCBI] 1.7208e-05
OPTB1 [NCBI] 1.55164e-05
ABS [NCBI] 1.45749e-05
EBR1 [NCBI] 1.45749e-05
CHNG2 [NCBI] 1.41327e-05
PTHLH [NCBI] 1.36624e-05
pfeiffer syndrome [NCBI] 1.32997e-05
PKS [NCBI] 1.32997e-05
mucopolysaccharidosis type vii [NCBI] 1.32997e-05
SRY [NCBI] 1.18144e-05
CDPX2 [NCBI] 1.18113e-05
RBS [NCBI] 1.14715e-05
IHH [NCBI] 1.13098e-05
TRPS2 [NCBI] 9.93408e-06
AIRE [NCBI] 9.87446e-06
FGFR1 [NCBI] 9.67716e-06
GCPS [NCBI] 9.38529e-06
GUSB [NCBI] 9.11697e-06
ACP5 [NCBI] 7.26865e-06
mucolipidosis ii [NCBI] 6.88618e-06
BGLAP [NCBI] 6.80569e-06
osteogenesis imperfecta, type iia [NCBI] 6.15143e-06
glioma of brain, familial [NCBI] 5.8122e-06
SDC2 [NCBI] 5.33889e-06
GPI [NCBI] 4.23929e-06
osteogenesis imperfecta, type i [NCBI] 2.92439e-06
CCD [NCBI] 2.92439e-06
APS1 [NCBI] 1.50608e-06
GAPDH [NCBI] 9.18214e-07
DBA [NCBI] 6.78337e-07
CPI [NCBI] 3.73849e-07
leber optic atrophy [NCBI] 1.20628e-07



Database Center for Life Science