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01 Hand [NCBI]


Gene


Gene Link Information
Gain
01
MS [NCBI] 0.00080315
OA8 [NCBI] 0.000367171
OA18 [NCBI] 0.000367171
OA6 [NCBI] 0.000367171
OA2 [NCBI] 0.000367171
OA9 [NCBI] 0.000367171
OA7 [NCBI] 0.000367171
OA5 [NCBI] 0.000367171
OA4 [NCBI] 0.000367171
OA20 [NCBI] 0.000367171
OA3 [NCBI] 0.000367171
OA19 [NCBI] 0.000367171
HSR [NCBI] 0.000367171
OA1 [NCBI] 0.000367171
ZLS [NCBI] 0.000295279
SHFM2 [NCBI] 0.000268171
WDM [NCBI] 0.000250581
FOP [NCBI] 0.000136017
MATN1 [NCBI] 2.70247e-05
BSCL2 [NCBI] 2.68564e-05
SHOX [NCBI] 2.23549e-05
COMP [NCBI] 1.84601e-05
GNB3 [NCBI] 1.72684e-05
MATN3 [NCBI] 1.34082e-05
IL1RN [NCBI] 1.17855e-05
HFE [NCBI] 1.14602e-05
CHI3L1 [NCBI] 8.62709e-06
COL2A1 [NCBI] 8.41438e-06
MITF [NCBI] 7.47813e-06
PTH [NCBI] 7.08313e-06
IL27RA [NCBI] 6.21861e-06
SLC39A4 [NCBI] 5.96702e-06
SPG20 [NCBI] 5.96702e-06
MAD2L1BP [NCBI] 5.89551e-06
PLOD2 [NCBI] 5.59911e-06
ADCY6 [NCBI] 5.37086e-06
WISP3 [NCBI] 5.29241e-06
WISP1 [NCBI] 5.29241e-06
PNPLA2 [NCBI] 5.25539e-06
ADRA2B [NCBI] 5.15191e-06
CTGF [NCBI] 5.15076e-06
ANKH [NCBI] 5.11967e-06
SERPINH1 [NCBI] 5.08845e-06
DSC3 [NCBI] 5.05817e-06
NSD1 [NCBI] 4.9455e-06
GAP43 [NCBI] 4.84428e-06
HSPB8 [NCBI] 4.82051e-06
DKK3 [NCBI] 4.82051e-06
SLC26A2 [NCBI] 4.73072e-06
HLA-DMA [NCBI] 4.70948e-06
DSC1 [NCBI] 4.70948e-06
FTL [NCBI] 4.68869e-06
HLA-DMB [NCBI] 4.66832e-06
ARX [NCBI] 4.64837e-06
KCNA1 [NCBI] 4.38899e-06
NOV [NCBI] 4.30165e-06
PANK2 [NCBI] 4.22138e-06
LOX [NCBI] 4.18356e-06
FBN1 [NCBI] 4.13528e-06
TIMP2 [NCBI] 4.10056e-06
CD68 [NCBI] 4.07935e-06
SOX10 [NCBI] 3.9929e-06
MAOA [NCBI] 3.92396e-06
NOS3 [NCBI] 3.90675e-06
TOR1A [NCBI] 3.85066e-06
DSG1 [NCBI] 3.83315e-06
HTR1B [NCBI] 3.7033e-06
DKK1 [NCBI] 3.66601e-06
SMN2 [NCBI] 3.61606e-06
TIMP1 [NCBI] 3.60913e-06
JUP [NCBI] 3.52955e-06
CTNNB1 [NCBI] 3.49583e-06
CD163 [NCBI] 3.46188e-06
ADAR [NCBI] 3.45596e-06
FGF23 [NCBI] 3.40418e-06
DSP [NCBI] 3.40418e-06
ADRB2 [NCBI] 3.36036e-06
IL1A [NCBI] 3.30314e-06
SMN1 [NCBI] 3.2782e-06
PAX3 [NCBI] 3.23487e-06
HLA-DRB1 [NCBI] 3.09478e-06
DMPK [NCBI] 3.02028e-06
ETV6 [NCBI] 2.99055e-06
MECP2 [NCBI] 2.97603e-06
KRT20 [NCBI] 2.94761e-06
CFTR [NCBI] 2.8442e-06
BDNF [NCBI] 2.79451e-06
PMP22 [NCBI] 2.71836e-06
PARK2 [NCBI] 2.56132e-06
HSPB1 [NCBI] 2.55899e-06
IL1B [NCBI] 2.48729e-06
COMT [NCBI] 2.34173e-06
IBSP [NCBI] 2.32164e-06
CCL11 [NCBI] 2.26047e-06
TNF [NCBI] 2.17746e-06
TGFBR1 [NCBI] 2.17186e-06
SLC2A1 [NCBI] 2.13868e-06
PTPN11 [NCBI] 2.13278e-06
TNFRSF11B [NCBI] 2.01044e-06
TNFRSF11A [NCBI] 1.95316e-06
FOXP3 [NCBI] 1.86155e-06
TNFSF11 [NCBI] 1.8337e-06
IL6 [NCBI] 1.82322e-06
ACP5 [NCBI] 1.77954e-06
CTSL1 [NCBI] 1.7648e-06
VDR [NCBI] 1.74743e-06
PTEN [NCBI] 1.66547e-06
APOE [NCBI] 1.38825e-06
LIF [NCBI] 1.31563e-06
MBP [NCBI] 1.0288e-06
CHAT [NCBI] 1.0288e-06
AVP [NCBI] 8.70788e-07
VIP [NCBI] 7.34076e-07
GFAP [NCBI] 6.64018e-07
EGFR [NCBI] 6.4413e-07
ACHE [NCBI] 6.35391e-07
TH [NCBI] 5.70045e-07
NPY [NCBI] 4.92986e-07




OMIM


OMIM Link Information
gain
01
RA [NCBI] 0.0044413
acroosteolysis with osteoporosis and changes in skull and mandible [NCBI] 0.00204182
amyotrophy, monomelic [NCBI] 0.00195814
mohr syndrome [NCBI] 0.00195814
CTS1 [NCBI] 0.00188416
upington disease [NCBI] 0.00110106
spondylometaphyseal dysplasia, type a4 [NCBI] 0.00110106
brachydactyly, type a5, with nail dysplasia [NCBI] 0.00110106
SHFLD1 [NCBI] 0.00105133
fingerprints, absence of [NCBI] 0.000791708
dermal ridges-off-the-end [NCBI] 0.000791708
osteodysplasia, familial, anderson type [NCBI] 0.000791708
MPD3 [NCBI] 0.000791708
dyschromatosis universalis hereditaria [NCBI] 0.000791708
clubbing of digits [NCBI] 0.000791708
MF4 [NCBI] 0.000675971
spondylometaphyseal dysplasia, corner fracture type [NCBI] 0.000675971
epidermolysis bullosa inversa dystrophica [NCBI] 0.000675971
spondyloepiphyseal dysplasia tarda, autosomal dominant [NCBI] 0.000675971
SHFM1 [NCBI] 0.000647829
CF [NCBI] 0.000618253
keratolytic winter erythema [NCBI] 0.000601389
dupuytren contracture [NCBI] 0.000601389
brachydactyly-mental retardation syndrome [NCBI] 0.000601389
SHFM2 [NCBI] 0.000601389
dermal ridges, patternless [NCBI] 0.000601389
epiphyseal dysplasia, microcephaly, and nystagmus [NCBI] 0.000546353
hereditary motor and sensory neuropathy v [NCBI] 0.000502829
camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases [NCBI] 0.000502829
hand clasping pattern [NCBI] 0.000490195
stiff skin syndrome [NCBI] 0.000466912
HOA [NCBI] 0.000453079
ZLS [NCBI] 0.000409934
DBQD [NCBI] 0.000386605
WDM [NCBI] 0.000386605
osteolysis, hereditary, of carpal bones with nephropathy [NCBI] 0.000386605
varadi-papp syndrome [NCBI] 0.000329941
tetramelic monodactyly [NCBI] 0.000280286
HSR [NCBI] 0.00024452
proteus syndrome [NCBI] 0.000232125
SPD1 [NCBI] 0.000231166
acrogeria, gottron type [NCBI] 0.000226385
osteoarthritis [NCBI] 0.000223586
apnea, obstructive sleep [NCBI] 0.000219316
renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia [NCBI] 0.00018555
EEC1 [NCBI] 0.000177777
poland syndrome [NCBI] 0.000159507
SPG17 [NCBI] 0.000154036
spondyloepimetaphyseal dysplasia, strudwick type [NCBI] 0.000140122
osteolysis, hereditary multicentric [NCBI] 0.000140104
metachondromatosis [NCBI] 0.000140104
tendons, extensor, of fingers, anomalous insertion of [NCBI] 0.000140104
angiolipomatosis, familial [NCBI] 0.000140104
dermatoglyphics--palmar triradius d, absence of [NCBI] 0.000140104
eiken skeletal dysplasia [NCBI] 0.000140104
acrorenal syndrome [NCBI] 0.000140104
dermatoglyphics--hypothenar radial arch [NCBI] 0.000140104
palmomental reflex [NCBI] 0.000140104
adactylia, unilateral [NCBI] 0.000140104
symphalangism with multiple anomalies of hands and feet [NCBI] 0.000140104
arm folding preference [NCBI] 0.000140104
AOS [NCBI] 0.000129142
DMC [NCBI] 0.000129115
dyschromatosis symmetrica hereditaria 1 [NCBI] 0.000124374
SYM1 [NCBI] 0.00012003
LRS1 [NCBI] 0.00010885
pfeiffer syndrome [NCBI] 0.00010885
SLSN1 [NCBI] 0.00010885
PPAC [NCBI] 0.00010885
SLE [NCBI] 0.00010823
acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia [NCBI] 0.000101029
congenital disorder of glycosylation, type i/iix [NCBI] 0.000101029
chondrocalcinosis due to apatite crystal deposition [NCBI] 0.000101029
prader-willi habitus, osteopenia, and camptodactyly [NCBI] 0.000101029
acrocephalopolydactylous dysplasia [NCBI] 0.000101029
spondylometaphyseal dysplasia, east african type [NCBI] 0.000101029
achard syndrome [NCBI] 0.000101029
fingers, relative length of [NCBI] 0.000101029
dermal ridges, nelson syndrome [NCBI] 0.000101029
median-ulnar nerve communications [NCBI] 0.000101029
ulna metaphyseal dysplasia syndrome [NCBI] 0.000101029
puerto rican infant hypotonia syndrome [NCBI] 0.000101029
HCH [NCBI] 9.97061e-05
SEDC [NCBI] 9.97061e-05
COMP [NCBI] 9.72586e-05
COL2A1 [NCBI] 9.56667e-05
MG [NCBI] 9.25468e-05
brachydactyly, preaxial, with hallux varus and thumb abduction [NCBI] 8.6406e-05
melorheostosis [NCBI] 8.6406e-05
ankylosing vertebral hyperostosis with tylosis [NCBI] 8.6406e-05
ivic syndrome [NCBI] 8.6406e-05
TCC [NCBI] 8.6406e-05
SHFM4 [NCBI] 8.6406e-05
PRTS [NCBI] 8.6406e-05
DA2A [NCBI] 8.33321e-05
MATN3 [NCBI] 8.31786e-05
WS3 [NCBI] 7.69808e-05
roussy-levy hereditary areflexic dystasia [NCBI] 7.69808e-05
syndactyly, type iii [NCBI] 7.69808e-05
SMC [NCBI] 7.00241e-05
EDM4 [NCBI] 7.00241e-05
spondyloperipheral dysplasia [NCBI] 7.00241e-05
BCNS [NCBI] 6.93276e-05
enchondromatosis, multiple [NCBI] 6.45214e-05
BDE [NCBI] 6.45214e-05
DA1 [NCBI] 6.45214e-05
ruvalcaba syndrome [NCBI] 6.45214e-05
palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal [NCBI] 6.45214e-05
OSMED [NCBI] 6.45214e-05
hyperostosis corticalis generalisata [NCBI] 6.45214e-05
KAL1 [NCBI] 6.24565e-05
marshall-smith syndrome [NCBI] 5.99793e-05
TD2 [NCBI] 5.61201e-05
HOS [NCBI] 5.30187e-05
pycnodysostosis [NCBI] 5.27714e-05
SDS [NCBI] 5.11088e-05
buschke-ollendorff syndrome [NCBI] 4.9819e-05
BDB1 [NCBI] 4.9819e-05
vater association [NCBI] 4.9819e-05
PSACH [NCBI] 4.92896e-05
diastrophic dysplasia [NCBI] 4.71832e-05
OPD1 [NCBI] 4.71832e-05
hand-foot-uterus syndrome [NCBI] 4.71832e-05
SYNS1 [NCBI] 4.71832e-05
PDP [NCBI] 4.71832e-05
BST1 [NCBI] 4.5782e-05
sitosterolemia [NCBI] 4.48062e-05
HSAN2 [NCBI] 4.48062e-05
CMT1A [NCBI] 4.3545e-05
WISP3 [NCBI] 4.33367e-05
BDC [NCBI] 4.26446e-05
SLC39A4 [NCBI] 4.15188e-05
weaver syndrome [NCBI] 4.06652e-05
DRRS [NCBI] 4.06652e-05
FMD [NCBI] 4.06652e-05
trichodentoosseous syndrome [NCBI] 3.88419e-05
chondrodysplasia punctata, autosomal dominant [NCBI] 3.88419e-05
camurati-engelmann disease [NCBI] 3.88419e-05
apert syndrome [NCBI] 3.88419e-05
CACP [NCBI] 3.88419e-05
ADAR [NCBI] 3.69353e-05
SLC26A2 [NCBI] 3.61352e-05
SALL4 [NCBI] 3.47619e-05
PLOSL [NCBI] 3.41187e-05
mucolipidosis iiia [NCBI] 3.41187e-05
CCAL2 [NCBI] 3.41187e-05
MADA [NCBI] 3.14565e-05
TP73L [NCBI] 3.09721e-05
ARX [NCBI] 3.02725e-05
OFD1 [NCBI] 3.02415e-05
mucopolysaccharidosis type vi [NCBI] 2.9094e-05
PTHR1 [NCBI] 2.87756e-05
EBR1 [NCBI] 2.80079e-05
TRPS1 [NCBI] 2.80079e-05
protoporphyria, erythropoietic [NCBI] 2.75399e-05
ACLS [NCBI] 2.59993e-05
PD [NCBI] 2.59697e-05
PAX3 [NCBI] 2.41755e-05
MAOA [NCBI] 2.38994e-05
GNAS [NCBI] 2.37654e-05
LOX [NCBI] 2.27764e-05
breast cancer [NCBI] 2.17481e-05
MSD [NCBI] 2.10058e-05
LWD [NCBI] 2.10058e-05
TBS [NCBI] 1.96107e-05
LSA [NCBI] 1.89542e-05
hypophosphatemic rickets, x-linked dominant [NCBI] 1.89542e-05
CASR [NCBI] 1.89044e-05
CSA [NCBI] 1.83231e-05
FOP [NCBI] 1.83231e-05
sotos syndrome [NCBI] 1.77158e-05
CD [NCBI] 1.7373e-05
BGLAP [NCBI] 1.7071e-05
TRPS2 [NCBI] 1.54997e-05
RSTS [NCBI] 1.54997e-05
PMP22 [NCBI] 1.53947e-05
RTT [NCBI] 1.43288e-05
SRS [NCBI] 1.36234e-05
AKR1B1 [NCBI] 1.32559e-05
SDC2 [NCBI] 1.19926e-05
CLS [NCBI] 1.11288e-05
neuraminidase deficiency [NCBI] 1.07645e-05
TD1 [NCBI] 1.04112e-05
AHO [NCBI] 1.00687e-05
PTH [NCBI] 9.85937e-06
mucolipidosis ii [NCBI] 9.10128e-06
EV [NCBI] 7.66911e-06
CCD [NCBI] 6.43124e-06
TNFRSF11B [NCBI] 6.36325e-06
VDR [NCBI] 5.0021e-06
PWS [NCBI] 3.93378e-06
temporal arteritis [NCBI] 3.31243e-06
NPPA [NCBI] 2.42826e-06
fragile x mental retardation syndrome [NCBI] 1.72887e-06
SMS [NCBI] 1.16256e-06
MBP [NCBI] 1.06821e-06
CHAT [NCBI] 1.01103e-06
DFSP [NCBI] 9.60685e-07
TNF [NCBI] 8.63125e-07
BDNF [NCBI] 3.26714e-07
VIP [NCBI] 1.58341e-07
AVP [NCBI] 1.46727e-07
GFAP [NCBI] 5.77428e-08
NPY [NCBI] 4.75035e-08
ACHE [NCBI] 3.0454e-08
dystrophia myotonica 1 [NCBI] 2.95192e-08
VEGF [NCBI] 6.33363e-09
TH [NCBI] 2.7532e-11




Database Center for Life Science