Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Calcinosis [NCBI]


Gene


Gene Link Information
Gain
01
MGP [NCBI] 0.00107743
IBGC1 [NCBI] 0.000686903
FOP [NCBI] 0.000292579
SCA20 [NCBI] 0.000281036
AGS2 [NCBI] 0.000281036
C5orf26 [NCBI] 0.000258126
MNG1 [NCBI] 0.000258126
TNFRSF11B [NCBI] 0.000234432
PTH [NCBI] 0.000233972
FGF23 [NCBI] 0.000211943
BMP2 [NCBI] 0.000137128
ENPP1 [NCBI] 0.000123928
AHSG [NCBI] 0.000108299
CA2 [NCBI] 7.95411e-05
IBSP [NCBI] 5.96326e-05
GALNT3 [NCBI] 5.91508e-05
REG1A [NCBI] 5.1065e-05
TNFRSF11A [NCBI] 5.07684e-05
BMP4 [NCBI] 4.99555e-05
TNFSF11 [NCBI] 4.23529e-05
BMP7 [NCBI] 3.97954e-05
ANKH [NCBI] 3.78787e-05
RUNX2 [NCBI] 3.50953e-05
TREX1 [NCBI] 3.46124e-05
SAMD9 [NCBI] 3.00184e-05
ADM [NCBI] 2.85358e-05
SPINK1 [NCBI] 2.68812e-05
SOX9 [NCBI] 2.65774e-05
PTHLH [NCBI] 2.46213e-05
MS [NCBI] 2.28406e-05
ABCC6 [NCBI] 2.16359e-05
ACP5 [NCBI] 1.92555e-05
SLC20A1 [NCBI] 1.89247e-05
CTSB [NCBI] 1.73315e-05
GNAS [NCBI] 1.72377e-05
RNASEH2A [NCBI] 1.68941e-05
GAS6 [NCBI] 1.56316e-05
CD68 [NCBI] 1.49245e-05
TREM2 [NCBI] 1.39907e-05
ACE [NCBI] 1.39161e-05
EPHX2 [NCBI] 1.36801e-05
AXL [NCBI] 1.36801e-05
COL10A1 [NCBI] 1.33956e-05
PNLIPRP2 [NCBI] 1.27376e-05
KL [NCBI] 1.26627e-05
SPP1 [NCBI] 1.23169e-05
ECM1 [NCBI] 1.14731e-05
TYROBP [NCBI] 1.13224e-05
TAGLN [NCBI] 1.05973e-05
LRRC18 [NCBI] 1.03581e-05
RNASEH2C [NCBI] 9.46064e-06
VKORC1 [NCBI] 8.95294e-06
CRP [NCBI] 8.67817e-06
GPR35 [NCBI] 8.44533e-06
AGXT2L1 [NCBI] 8.24632e-06
AP1S2 [NCBI] 8.1006e-06
POU1F1 [NCBI] 7.86617e-06
CTHRC1 [NCBI] 7.8141e-06
UMOD [NCBI] 7.71437e-06
HEY2 [NCBI] 7.3548e-06
TNNI1 [NCBI] 7.3548e-06
VDR [NCBI] 7.25269e-06
COL2A1 [NCBI] 7.24125e-06
NUMB [NCBI] 6.69614e-06
ABI2 [NCBI] 6.69614e-06
ALPPL2 [NCBI] 6.69614e-06
CILP [NCBI] 6.56495e-06
CA12 [NCBI] 6.44322e-06
DNAH5 [NCBI] 6.32968e-06
ESM1 [NCBI] 6.12328e-06
AMBN [NCBI] 6.12328e-06
LECT1 [NCBI] 5.93948e-06
POU3F4 [NCBI] 5.93948e-06
ESR2 [NCBI] 5.9018e-06
PTGDS [NCBI] 5.69679e-06
LMNA [NCBI] 5.61833e-06
TGFB1 [NCBI] 5.54172e-06
CCL2 [NCBI] 5.45207e-06
NOTCH1 [NCBI] 5.37119e-06
MEPE [NCBI] 5.35731e-06
MATN1 [NCBI] 5.23891e-06
CLCN5 [NCBI] 5.23881e-06
ATN1 [NCBI] 5.23881e-06
CPT2 [NCBI] 5.18259e-06
EBP [NCBI] 5.12822e-06
CST3 [NCBI] 5.08541e-06
CTSC [NCBI] 5.07558e-06
MMP13 [NCBI] 5.00132e-06
LBR [NCBI] 4.88037e-06
RECQL4 [NCBI] 4.74782e-06
ACVR1 [NCBI] 4.58629e-06
SNCA [NCBI] 4.58529e-06
EGR1 [NCBI] 4.55371e-06
STC1 [NCBI] 4.54829e-06
F12 [NCBI] 4.54829e-06
PTPN1 [NCBI] 4.54829e-06
TGFB3 [NCBI] 4.47486e-06
BMPR1A [NCBI] 4.43935e-06
CCL26 [NCBI] 4.4046e-06
CSF1 [NCBI] 4.4046e-06
FGG [NCBI] 4.37059e-06
PLA2G7 [NCBI] 4.33727e-06
S100A12 [NCBI] 4.24127e-06
LRP5 [NCBI] 4.21049e-06
LEP [NCBI] 4.13298e-06
ENPP2 [NCBI] 4.12157e-06
TNNI3 [NCBI] 4.09299e-06
AOC3 [NCBI] 4.01021e-06
BMP6 [NCBI] 3.90612e-06
CCR2 [NCBI] 3.8791e-06
ENG [NCBI] 3.85308e-06
ADAR [NCBI] 3.73898e-06
TFE3 [NCBI] 3.67244e-06
FGA [NCBI] 3.54731e-06
PANK2 [NCBI] 3.41303e-06
PRSS2 [NCBI] 3.34124e-06
HLA-DPB1 [NCBI] 3.22319e-06
GAA [NCBI] 3.20705e-06
ERCC6 [NCBI] 3.08377e-06
VWF [NCBI] 3.03034e-06
TGM2 [NCBI] 3.02572e-06
LIPC [NCBI] 3.02572e-06
ACVRL1 [NCBI] 3.02572e-06
CTGF [NCBI] 3.02525e-06
PLTP [NCBI] 2.98362e-06
TNFSF10 [NCBI] 2.98056e-06
PRSS1 [NCBI] 2.96985e-06
SFN [NCBI] 2.94268e-06
GATA3 [NCBI] 2.87687e-06
FOSL1 [NCBI] 2.87687e-06
CD40 [NCBI] 2.76535e-06
ADH1B [NCBI] 2.7069e-06
TCF7L2 [NCBI] 2.67293e-06
NPPB [NCBI] 2.66178e-06
NOG [NCBI] 2.63974e-06
CD40LG [NCBI] 2.62885e-06
SELE [NCBI] 2.6073e-06
ERCC5 [NCBI] 2.6073e-06
PIP [NCBI] 2.59665e-06
CNN1 [NCBI] 2.57559e-06
NLRP3 [NCBI] 2.57559e-06
BMPR2 [NCBI] 2.56517e-06
TIMP1 [NCBI] 2.54456e-06
CXCL9 [NCBI] 2.36251e-06
GPX1 [NCBI] 2.32705e-06
PCNA [NCBI] 2.12717e-06
CXCL10 [NCBI] 2.07968e-06
STK11 [NCBI] 2.02265e-06
MMP3 [NCBI] 2.0157e-06
APOE [NCBI] 1.95571e-06
BAD [NCBI] 1.94155e-06
HLA-C [NCBI] 1.93501e-06
APOD [NCBI] 1.87767e-06
RETN [NCBI] 1.77599e-06
CFTR [NCBI] 1.58959e-06
OSM [NCBI] 1.54178e-06
ICAM1 [NCBI] 1.53707e-06
CD99 [NCBI] 1.53237e-06
ERBB4 [NCBI] 1.4775e-06
ALDH2 [NCBI] 1.47305e-06
CTLA4 [NCBI] 1.35501e-06
PRKCA [NCBI] 1.34308e-06
TNF [NCBI] 1.31615e-06
LDLR [NCBI] 1.25946e-06
HLA-A [NCBI] 1.23419e-06
ALK [NCBI] 1.20258e-06
KRT7 [NCBI] 1.19226e-06
MEN1 [NCBI] 1.15529e-06
ALB [NCBI] 1.13892e-06
EGF [NCBI] 1.11761e-06
CCR5 [NCBI] 1.05203e-06
SLC2A1 [NCBI] 1.00854e-06
FAS [NCBI] 1.0029e-06
IGF1 [NCBI] 9.72444e-07
HLA-B [NCBI] 9.24736e-07
EGFR [NCBI] 9.23396e-07
PTGS2 [NCBI] 9.00952e-07
APP [NCBI] 8.99308e-07
IL8 [NCBI] 8.15861e-07
TLR2 [NCBI] 7.21879e-07
AGT [NCBI] 7.17868e-07
GJB2 [NCBI] 5.71907e-07
APOB [NCBI] 5.67063e-07
LIF [NCBI] 5.38755e-07
ESR1 [NCBI] 4.77436e-07
BRAF [NCBI] 4.73295e-07
CASP3 [NCBI] 4.23454e-07
HLA-DQB1 [NCBI] 4.10997e-07
CETP [NCBI] 3.46903e-07
GFAP [NCBI] 2.6195e-07
IL10 [NCBI] 2.31513e-07
PRL [NCBI] 2.16663e-07
TRH [NCBI] 1.72853e-07
VEGFA [NCBI] 1.52102e-07
TLR4 [NCBI] 1.28913e-07
HLA-DRB1 [NCBI] 1.28913e-07
HRAS [NCBI] 1.05064e-07
BDNF [NCBI] 8.30174e-08
AR [NCBI] 7.17036e-08
BAX [NCBI] 5.58303e-08
LPL [NCBI] 4.86003e-08
IL6 [NCBI] 4.86003e-08
AVP [NCBI] 4.49106e-08
NOS3 [NCBI] 2.40204e-08
CDKN1A [NCBI] 2.79139e-09
NOS2 [NCBI] 1.7398e-09




OMIM


OMIM Link Information
gain
01
IBGC1 [NCBI] 0.0166937
basal ganglia calcification, idiopathic, childhood-onset [NCBI] 0.00754944
basal ganglia calcification, idiopathic, 2 [NCBI] 0.00319562
HFTC [NCBI] 0.00285831
GACI [NCBI] 0.0019565
singleton-merten syndrome [NCBI] 0.00159232
scleroderma, familial progressive [NCBI] 0.0015144
AGS1 [NCBI] 0.00151393
folic acid, transport defect involving [NCBI] 0.00149767
intestinal atresia, multiple [NCBI] 0.00129807
PXE [NCBI] 0.0010891
TNFRSF11B [NCBI] 0.000870883
SPP1 [NCBI] 0.000798409
upington disease [NCBI] 0.000794815
cardiomyopathy, fatal fetal, due to myocardial calcification [NCBI] 0.000794815
PTH [NCBI] 0.00078125
OPTB3 [NCBI] 0.000773353
GALNT3 [NCBI] 0.000579385
3-@hydroxyisobutyric aciduria [NCBI] 0.000577852
RA [NCBI] 0.000527653
SCA20 [NCBI] 0.000496582
testicular microlithiasis [NCBI] 0.000496582
calcific aortic disease with immunologic abnormalities, familial [NCBI] 0.000457573
MVP [NCBI] 0.000436515
dentin dysplasia, type i [NCBI] 0.000405426
apnea, obstructive sleep [NCBI] 0.00039856
angioma, hereditary neurocutaneous [NCBI] 0.000374765
gaucher disease, type iiic [NCBI] 0.000371949
MNG1 [NCBI] 0.000349436
FGF23 [NCBI] 0.000345702
HHS [NCBI] 0.000335053
aortic aneurysm, familial thoracic 1 [NCBI] 0.000309189
keutel syndrome [NCBI] 0.000288635
kenny-caffey syndrome, type 2 [NCBI] 0.000277931
NFTC [NCBI] 0.00027439
spondyloenchondrodysplasia [NCBI] 0.000252498
RNS [NCBI] 0.000236393
pulmonary alveolar microlithiasis [NCBI] 0.00023075
tropical calcific pancreatitis [NCBI] 0.000219955
PCTT [NCBI] 0.000207261
ST8 [NCBI] 0.000204568
CF [NCBI] 0.000199815
SPARC [NCBI] 0.000191185
choroid plexus calcification and mental retardation [NCBI] 0.000182875
encephalopathy with intracranial calcification, growth hormone deficiency, microcephaly, and retinal degeneration [NCBI] 0.000182875
epilepsy with bilateral occipital calcifications [NCBI] 0.000182875
CCAL2 [NCBI] 0.000176476
hydrops-ectopic calcification-moth-eaten skeletal dysplasia [NCBI] 0.000175766
spondylometaepiphyseal dysplasia, short limb-hand type [NCBI] 0.000151978
amyloidosis, cerebroarterial, hereditary, iowa type [NCBI] 0.000151978
ossified ear cartilages with mental deficiency, muscle wasting, and bony changes [NCBI] 0.000151978
ADM [NCBI] 0.000134218
lipoid proteinosis of urbach and wiethe [NCBI] 0.000126949
SAMD9 [NCBI] 0.000109476
TRS [NCBI] 0.000105996
MGP [NCBI] 0.000100912
BCNS [NCBI] 0.000100879
OPLL [NCBI] 9.88457e-05
ENPP1 [NCBI] 9.72502e-05
craniosynostosis, calcification of basal ganglia, and facial dysmorphism [NCBI] 9.14121e-05
tracheopathia osteoplastica [NCBI] 9.14121e-05
diabetes insipidus, nephrogenic, with mental retardation and intracerebral calcification [NCBI] 9.14121e-05
vascular hyalinosis [NCBI] 9.14121e-05
hypophosphatemia, renal, with intracerebral calcifications [NCBI] 9.14121e-05
facial dysmorphism, selective tooth agenesis, and choroid calcification [NCBI] 9.14121e-05
arthropathy, tendinous calcinosis, and progeroid features [NCBI] 9.14121e-05
coracoclavicular joint, anomalous [NCBI] 9.14121e-05
hyperparathyroidism, neonatal self-limited primary, with hypercalciuria [NCBI] 9.14121e-05
wolman disease [NCBI] 8.44909e-05
ossified ear cartilages [NCBI] 6.89971e-05
AGS2 [NCBI] 6.89971e-05
revesz syndrome [NCBI] 6.89971e-05
chondrocalcinosis due to apatite crystal deposition [NCBI] 6.89971e-05
chondrodysplasia punctata syndrome [NCBI] 6.89971e-05
ulna metaphyseal dysplasia syndrome [NCBI] 6.89971e-05
dyschromatosis symmetrica hereditaria 1 [NCBI] 6.75738e-05
KL [NCBI] 6.74642e-05
VEGF [NCBI] 6.65953e-05
HHT [NCBI] 6.51864e-05
GBA [NCBI] 6.46391e-05
HRPT1 [NCBI] 6.4329e-05
CTHRC1 [NCBI] 6.41994e-05
thalamic degeneration, symmetric infantile [NCBI] 6.05726e-05
arthrogryposis multiplex congenita with whistling face [NCBI] 6.05726e-05
AD [NCBI] 5.96466e-05
RCDP1 [NCBI] 5.87611e-05
CHBL [NCBI] 5.51219e-05
haw river syndrome [NCBI] 5.51219e-05
carotid intimal medial thickness 1 [NCBI] 5.51219e-05
PKDTS [NCBI] 5.51219e-05
coronary heart disease, susceptibility to, 5 [NCBI] 5.51219e-05
metachondromatosis [NCBI] 5.51219e-05
BGLAP [NCBI] 5.43791e-05
ABCC6 [NCBI] 5.33252e-05
MRX59 [NCBI] 5.10836e-05
RNASEH2B [NCBI] 5.04342e-05
RNASEH2C [NCBI] 5.04342e-05
pilomatrixoma [NCBI] 4.78772e-05
MG [NCBI] 4.63258e-05
ARNTL [NCBI] 4.52483e-05
RNASEH2A [NCBI] 4.52483e-05
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation [NCBI] 4.52204e-05
EKD1 [NCBI] 4.51097e-05
aortic valve disease [NCBI] 4.45613e-05
carnitine palmitoyltransferase ii deficiency, lethal neonatal [NCBI] 4.29543e-05
PBC [NCBI] 4.29543e-05
SLC34A2 [NCBI] 4.1886e-05
HEY2 [NCBI] 4.1886e-05
AP1S2 [NCBI] 4.1886e-05
AHSG [NCBI] 4.1886e-05
osseous heteroplasia, progressive [NCBI] 4.09804e-05
EPHX2 [NCBI] 3.93899e-05
dentinogenesis imperfecta, shields type iii [NCBI] 3.92331e-05
BPP [NCBI] 3.92331e-05
EGF [NCBI] 3.86152e-05
OSMED [NCBI] 3.7667e-05
SLC22A6 [NCBI] 3.74038e-05
FOP [NCBI] 3.64665e-05
gaucher disease, type i [NCBI] 3.61057e-05
TREM2 [NCBI] 3.57548e-05
HOMG [NCBI] 3.49542e-05
NSHPT [NCBI] 3.49542e-05
HHS [NCBI] 3.37637e-05
vitamin k-dependent clotting factors, combined deficiency of, 1 [NCBI] 3.37637e-05
LMNA [NCBI] 3.34563e-05
ANKH [NCBI] 3.20239e-05
TREX1 [NCBI] 3.20239e-05
dent disease 1 [NCBI] 3.16386e-05
marshall syndrome [NCBI] 3.16386e-05
chondrodysplasia punctata, autosomal dominant [NCBI] 3.16386e-05
molybdenum cofactor deficiency [NCBI] 3.16386e-05
DGI1 [NCBI] 3.16386e-05
CA2 [NCBI] 3.10437e-05
SLC6A6 [NCBI] 3.10437e-05
PPCD1 [NCBI] 2.9786e-05
CPT2 [NCBI] 2.93406e-05
CSF1 [NCBI] 2.85907e-05
CTSB [NCBI] 2.85907e-05
PLOSL [NCBI] 2.81467e-05
PALS [NCBI] 2.73935e-05
EGFR [NCBI] 2.64798e-05
LBR [NCBI] 2.55353e-05
NOTCH1 [NCBI] 2.45458e-05
VWM [NCBI] 2.41433e-05
PHA [NCBI] 2.41433e-05
ACP5 [NCBI] 2.4024e-05
biotinidase deficiency [NCBI] 2.30345e-05
BMP2 [NCBI] 2.28358e-05
phenylketonuria ii [NCBI] 2.28358e-05
PDB [NCBI] 2.25131e-05
alkaptonuria [NCBI] 2.25131e-05
bartter syndrome, type 3 [NCBI] 2.10636e-05
CTSC [NCBI] 2.07514e-05
MMP3 [NCBI] 2.07514e-05
EFE [NCBI] 2.06146e-05
MCOPS7 [NCBI] 2.06146e-05
CYP1A1 [NCBI] 2.01731e-05
TNF [NCBI] 1.9846e-05
GAA [NCBI] 1.95885e-05
ODDD [NCBI] 1.93563e-05
hypophosphatasia, infantile [NCBI] 1.89636e-05
FIH [NCBI] 1.89636e-05
UMOD [NCBI] 1.88063e-05
KSS [NCBI] 1.87335e-05
PRL [NCBI] 1.82104e-05
PTHLH [NCBI] 1.78857e-05
exostoses, multiple, type i [NCBI] 1.78562e-05
CNC1 [NCBI] 1.78562e-05
HHC1 [NCBI] 1.71708e-05
CALCRL [NCBI] 1.70085e-05
melanoma, uveal [NCBI] 1.53278e-05
TS [NCBI] 1.45674e-05
hypophosphatemic rickets, x-linked dominant [NCBI] 1.45081e-05
STAT1 [NCBI] 1.41173e-05
CSA [NCBI] 1.39938e-05
mucolipidosis ii [NCBI] 1.32661e-05
osteogenesis imperfecta, type iia [NCBI] 1.23687e-05
MTTL1 [NCBI] 1.18816e-05
GNAS [NCBI] 1.17744e-05
CRMO [NCBI] 1.13492e-05
CLS [NCBI] 1.13492e-05
CEACAM5 [NCBI] 1.13401e-05
hurler syndrome [NCBI] 1.11575e-05
MUC1 [NCBI] 9.90554e-06
PLTP [NCBI] 9.90426e-06
SLE [NCBI] 9.53985e-06
HGPS [NCBI] 9.43125e-06
SVAS [NCBI] 8.39789e-06
AR [NCBI] 7.86811e-06
AGER [NCBI] 7.85762e-06
AVP [NCBI] 7.40161e-06
SDS [NCBI] 7.3593e-06
CD [NCBI] 7.3536e-06
glycogen storage disease ii [NCBI] 7.23888e-06
temporal arteritis [NCBI] 7.18474e-06
SPINK1 [NCBI] 6.50468e-06
AHO [NCBI] 6.3419e-06
APP [NCBI] 6.31451e-06
OSM [NCBI] 6.08556e-06
krabbe disease [NCBI] 4.2987e-06
ALK [NCBI] 4.28831e-06
phenylketonuria [NCBI] 3.92923e-06
RB1 [NCBI] 3.81602e-06
LDLR [NCBI] 3.81602e-06
CFTR [NCBI] 3.79121e-06
GFAP [NCBI] 3.4662e-06
IP [NCBI] 3.35292e-06
LPL [NCBI] 2.4951e-06
DRPLA [NCBI] 2.43203e-06
EIG [NCBI] 2.38453e-06
APOE [NCBI] 2.13305e-06
BDNF [NCBI] 2.09312e-06
VDR [NCBI] 1.98773e-06
ALD [NCBI] 1.63945e-06
CTGF [NCBI] 1.4274e-06
leber optic atrophy [NCBI] 1.21117e-06
ALB [NCBI] 1.19231e-06
LAM [NCBI] 1.18179e-06
polycystic kidneys [NCBI] 8.91286e-07
WBS [NCBI] 8.64373e-07
PJS [NCBI] 4.47926e-07
GIST [NCBI] 1.18825e-07
MFS [NCBI] 9.188e-08
PCNA [NCBI] 2.52226e-08




Database Center for Life Science