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MeSH keywords -> Related genes, diseases (OMIM)


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01 Connective Tissue Diseases [NCBI]


Gene


Gene Link Information
Gain
01
TROVE2 [NCBI] 0.000176955
COL2A1 [NCBI] 0.000131063
MS [NCBI] 5.28348e-05
SLC2A10 [NCBI] 4.43943e-05
COL3A1 [NCBI] 3.10317e-05
FBN1 [NCBI] 3.00616e-05
XRCC5 [NCBI] 2.32242e-05
COL11A1 [NCBI] 2.02761e-05
EXOSC10 [NCBI] 2.00214e-05
ANTXR2 [NCBI] 1.91582e-05
PSIP1 [NCBI] 1.75221e-05
NUMA1 [NCBI] 1.65959e-05
CENPB [NCBI] 1.52082e-05
ELN [NCBI] 1.42251e-05
TGFBR2 [NCBI] 1.35732e-05
PCNA [NCBI] 1.35326e-05
PLOD3 [NCBI] 1.26793e-05
POP1 [NCBI] 1.11978e-05
VWF [NCBI] 1.06997e-05
SLC20A1 [NCBI] 1.04187e-05
NUP153 [NCBI] 1.01315e-05
SNRPB2 [NCBI] 1.01315e-05
SNRPC [NCBI] 9.88558e-06
FBN2 [NCBI] 9.15191e-06
PIAS1 [NCBI] 8.87696e-06
TGFBR1 [NCBI] 8.80427e-06
RPP14 [NCBI] 8.53304e-06
SERPINH1 [NCBI] 8.33706e-06
MMP2 [NCBI] 8.26764e-06
COL6A2 [NCBI] 8.2469e-06
PEPD [NCBI] 8.2469e-06
ANTXR1 [NCBI] 8.00192e-06
LRP6 [NCBI] 7.92751e-06
DDX5 [NCBI] 7.92751e-06
CSPG4 [NCBI] 7.8562e-06
NUP210 [NCBI] 7.78776e-06
MUC1 [NCBI] 7.73757e-06
COL6A1 [NCBI] 7.65862e-06
SNRNP70 [NCBI] 7.65862e-06
TRPM6 [NCBI] 7.59754e-06
KIF11 [NCBI] 7.42647e-06
FBLN5 [NCBI] 7.22223e-06
LOXL1 [NCBI] 7.17479e-06
SP100 [NCBI] 6.95566e-06
FLNA [NCBI] 6.76163e-06
XRCC6 [NCBI] 6.72536e-06
TNXB [NCBI] 6.62099e-06
LOX [NCBI] 6.55482e-06
HAPLN1 [NCBI] 6.28551e-06
ENO1 [NCBI] 6.23109e-06
S100A6 [NCBI] 5.98261e-06
COL1A2 [NCBI] 5.59284e-06
COL11A2 [NCBI] 5.46943e-06
EDA [NCBI] 5.43579e-06
ACE [NCBI] 5.41932e-06
ABCC6 [NCBI] 5.32313e-06
HLA-DRB1 [NCBI] 5.32037e-06
NPPB [NCBI] 4.8759e-06
NF1 [NCBI] 4.86408e-06
BMPR2 [NCBI] 4.77241e-06
TIMP1 [NCBI] 4.75027e-06
PLAU [NCBI] 4.63359e-06
PLG [NCBI] 4.62339e-06
CASR [NCBI] 4.59315e-06
CCR4 [NCBI] 4.43168e-06
TNFSF13B [NCBI] 4.36092e-06
GNAS [NCBI] 4.23605e-06
COL1A1 [NCBI] 4.10536e-06
HLA-C [NCBI] 4.08336e-06
PTGS2 [NCBI] 4.063e-06
FGF23 [NCBI] 3.77336e-06
CTSG [NCBI] 3.63581e-06
CXCR3 [NCBI] 3.27954e-06
HLA-A [NCBI] 3.27085e-06
TPO [NCBI] 3.15416e-06
MPO [NCBI] 3.05156e-06
HLA-B [NCBI] 2.88336e-06
ADAMTS13 [NCBI] 2.7707e-06
FOXP3 [NCBI] 2.445e-06
CCL2 [NCBI] 2.19114e-06
PLAUR [NCBI] 1.78539e-06
CALCA [NCBI] 1.75726e-06
CAT [NCBI] 1.48355e-06
IL1RN [NCBI] 1.12801e-06
VEGFA [NCBI] 5.87843e-07
PRL [NCBI] 5.15106e-07
PTH [NCBI] 1.69051e-07
EGFR [NCBI] 1.61587e-07
TNF [NCBI] 6.45811e-08




OMIM


OMIM Link Information
gain
01
SLE [NCBI] 0.00313448
gapo syndrome [NCBI] 0.00138193
stiff skin syndrome [NCBI] 0.00130285
joint laxity, familial [NCBI] 0.000819746
camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases [NCBI] 0.000587372
AKE [NCBI] 0.000545541
ehlers-danlos syndrome, type vib [NCBI] 0.000512699
EPS [NCBI] 0.000509599
STL1 [NCBI] 0.000495753
skin creases, multiple benign ring-shaped, of limbs [NCBI] 0.000485681
ACG1A [NCBI] 0.000462747
RA [NCBI] 0.000401861
MVP [NCBI] 0.00033954
FBN1 [NCBI] 0.000296174
CF [NCBI] 0.000287174
proteus syndrome [NCBI] 0.00028611
OFC1 [NCBI] 0.00026551
COL2A1 [NCBI] 0.000265178
MFS [NCBI] 0.00018037
buschke-ollendorff syndrome [NCBI] 0.000141926
contractural arachnodactyly, congenital [NCBI] 0.000132949
STL2 [NCBI] 0.000117704
MFS2 [NCBI] 0.000108417
COL11A1 [NCBI] 0.000100331
ATS [NCBI] 9.54368e-05
harrod syndrome [NCBI] 9.26351e-05
hydrocephalus, tall stature, joint laxity, and kyphoscoliosis [NCBI] 9.26351e-05
osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones, but without fractures [NCBI] 9.26351e-05
ehlers-danlos syndrome, autosomal dominant, type unspecified [NCBI] 9.26351e-05
OPPG [NCBI] 8.63064e-05
SNRPB2 [NCBI] 7.85884e-05
POP1 [NCBI] 7.85884e-05
PPAC [NCBI] 7.62916e-05
UCMD [NCBI] 7.49027e-05
ELN [NCBI] 7.0404e-05
epiphyseal dysplasia, multiple, with myopia and conductive deafness [NCBI] 7.02159e-05
EXOSC10 [NCBI] 6.48113e-05
TNR [NCBI] 6.48113e-05
mass syndrome [NCBI] 6.17872e-05
hyperimmunoglobulin g1(a1) syndrome [NCBI] 6.17872e-05
heterotopia, periventricular, ehlers-danlos variant [NCBI] 5.63323e-05
acrogeria, gottron type [NCBI] 5.63323e-05
SLC2A10 [NCBI] 5.62393e-05
PXE [NCBI] 5.58424e-05
COL5A2 [NCBI] 5.37312e-05
CENPC1 [NCBI] 5.37312e-05
WISP3 [NCBI] 5.17332e-05
stickler syndrome, type i, nonsyndromic ocular [NCBI] 4.90792e-05
STL3 [NCBI] 4.90792e-05
MMP14 [NCBI] 4.63055e-05
TNXB [NCBI] 4.44121e-05
COL6A2 [NCBI] 4.44121e-05
COL11A2 [NCBI] 4.28246e-05
HGD [NCBI] 4.28246e-05
PCNA [NCBI] 4.25743e-05
AOII [NCBI] 4.21698e-05
weill-marchesani syndrome, autosomal recessive [NCBI] 4.04183e-05
FN1 [NCBI] 4.02585e-05
noonan-like/multiple giant cell lesion syndrome [NCBI] 3.8848e-05
shprintzen-goldberg craniosynostosis syndrome [NCBI] 3.8848e-05
PEPD [NCBI] 3.86961e-05
TNFSF13B [NCBI] 3.86961e-05
antiphospholipid syndrome [NCBI] 3.74258e-05
WSS [NCBI] 3.74258e-05
COL6A1 [NCBI] 3.73491e-05
TGFBR2 [NCBI] 3.65444e-05
WZS [NCBI] 3.61268e-05
LDS [NCBI] 3.61268e-05
complement component 2 deficiency [NCBI] 3.58009e-05
GLB1 [NCBI] 3.38607e-05
kniest dysplasia [NCBI] 3.38266e-05
WGN1 [NCBI] 3.38266e-05
LOX [NCBI] 3.30189e-05
FLNA [NCBI] 3.30189e-05
cutis laxa, autosomal recessive, type ii [NCBI] 3.27986e-05
mucopolysaccharidosis type iva [NCBI] 2.94634e-05
cutis laxa, autosomal recessive, type i [NCBI] 2.85325e-05
GABEB [NCBI] 2.71301e-05
cutis laxa, x-linked [NCBI] 2.58564e-05
alkaptonuria [NCBI] 2.36184e-05
ehlers-danlos syndrome, type i [NCBI] 1.96506e-05
COH1 [NCBI] 1.78889e-05
ACE [NCBI] 1.37944e-05
HGPS [NCBI] 1.03388e-05
SVAS [NCBI] 9.27604e-06
osteogenesis imperfecta, type i [NCBI] 8.99475e-06
MG [NCBI] 8.56853e-06
VEGF [NCBI] 8.34409e-06
SPP1 [NCBI] 7.05443e-06
MPO [NCBI] 5.82792e-06
FMF [NCBI] 5.66492e-06
polycystic kidneys [NCBI] 2.92958e-06
CAT [NCBI] 2.78825e-06
WBS [NCBI] 1.2541e-06
PTH [NCBI] 7.47815e-07
EGFR [NCBI] 2.76372e-07
CD [NCBI] 1.84692e-07
thrombocytopenic purpura, autoimmune [NCBI] 3.8771e-10
PRL [NCBI] 2.90647e-10




Database Center for Life Science