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MeSH keywords -> Related genes, diseases (OMIM)


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01 Collagen Diseases [NCBI]

Gene


 Gene Link Information
Gain		 01
VUR [NCBI] 9.28181e-05
COL2A1 [NCBI] 8.98753e-05
MS [NCBI] 7.55426e-05
MUC1 [NCBI] 7.10573e-05
COL1A2 [NCBI] 2.66539e-05
TROVE2 [NCBI] 2.54914e-05
COL1A1 [NCBI] 2.20681e-05
COL6A2 [NCBI] 2.17419e-05
COL3A1 [NCBI] 1.58469e-05
FCGBP [NCBI] 1.15084e-05
VWF [NCBI] 1.05287e-05
ADAMTS13 [NCBI] 1.04986e-05
LEMD3 [NCBI] 1.01302e-05
COL10A1 [NCBI] 9.16187e-06
COL6A1 [NCBI] 9.03243e-06
PSIP1 [NCBI] 8.9121e-06
COL4A4 [NCBI] 8.32741e-06
ADAMTS2 [NCBI] 7.32656e-06
COL7A1 [NCBI] 7.28131e-06
PPOX [NCBI] 7.07153e-06
COL4A5 [NCBI] 6.83264e-06
COL11A2 [NCBI] 6.83264e-06
HGF [NCBI] 6.59537e-06
VIM [NCBI] 6.43709e-06
FGF3 [NCBI] 6.43709e-06
CD40LG [NCBI] 6.19726e-06
AMBP [NCBI] 4.98672e-06
XRCC5 [NCBI] 4.79358e-06
HP [NCBI] 4.64375e-06
ALB [NCBI] 4.47291e-06
PTGS2 [NCBI] 3.84324e-06
CD38 [NCBI] 3.81902e-06
CCL2 [NCBI] 3.45981e-06
TNFRSF11B [NCBI] 3.38477e-06
ADA [NCBI] 3.28943e-06
PTHLH [NCBI] 3.18127e-06
TRH [NCBI] 2.93826e-06
CAT [NCBI] 2.68431e-06
PTEN [NCBI] 2.36958e-06
IL1RN [NCBI] 2.27539e-06
TGFB1 [NCBI] 1.8593e-06
TNF [NCBI] 1.82288e-06
FASLG [NCBI] 1.72678e-06
PRL [NCBI] 1.50344e-06



OMIM


 OMIM Link Information
gain		 01
collagenosis, familial reactive perforating [NCBI] 0.00572149
stiff skin syndrome [NCBI] 0.00143026
SLE [NCBI] 0.00135799
eosinophilia, familial [NCBI] 0.000705355
MVP [NCBI] 0.000398025
COL2A1 [NCBI] 0.00036355
cardiomyopathy-hypogonadism-collagenoma syndrome [NCBI] 0.000282396
ehlers-danlos syndrome, type vii, autosomal recessive [NCBI] 0.000279791
RA [NCBI] 0.000184409
EPS [NCBI] 0.000177219
ehlers-danlos syndrome, type vii, autosomal dominant [NCBI] 0.000125013
COL1A1 [NCBI] 0.000119773
heart block, congenital [NCBI] 0.000109179
alpha-2-deficient collagen disease [NCBI] 0.000106151
ehlers-danlos syndrome, beasley-cohen type [NCBI] 0.000106151
HFTC [NCBI] 9.2882e-05
SEDC [NCBI] 8.71069e-05
fascial dystrophy, congenital [NCBI] 8.37014e-05
COL1A2 [NCBI] 7.61166e-05
larsen-like syndrome, lethal type [NCBI] 7.52424e-05
spondylometaphyseal dysplasia with dentinogenesis imperfecta [NCBI] 7.52424e-05
FCGRT [NCBI] 6.51968e-05
hyalinosis, infantile systemic [NCBI] 6.24434e-05
marfanoid hypermobility syndrome [NCBI] 6.24434e-05
TROVE2 [NCBI] 6.18211e-05
osteogenesis imperfecta, type i [NCBI] 6.07362e-05
melorheostosis [NCBI] 5.74516e-05
PVOD [NCBI] 5.54431e-05
winchester syndrome [NCBI] 5.54431e-05
COL6A2 [NCBI] 4.99813e-05
kniest dysplasia [NCBI] 4.69181e-05
complement factor h deficiency [NCBI] 4.58597e-05
DCN [NCBI] 4.52677e-05
myasthenic syndrome, congenital, associated with episodic apnea [NCBI] 4.4869e-05
PLOD1 [NCBI] 4.33297e-05
buschke-ollendorff syndrome [NCBI] 4.22297e-05
cutis laxa, autosomal recessive, type i [NCBI] 4.1442e-05
COL10A1 [NCBI] 4.13449e-05
UCMD [NCBI] 3.92971e-05
ehlers-danlos syndrome, type vi [NCBI] 3.86447e-05
COL7A1 [NCBI] 3.6595e-05
DMPK [NCBI] 3.61621e-05
COL3A1 [NCBI] 3.55467e-05
ehlers-danlos syndrome, type i [NCBI] 3.20447e-05
STL1 [NCBI] 3.16412e-05
PXE [NCBI] 3.15563e-05
VIM [NCBI] 3.10223e-05
BTK [NCBI] 2.91086e-05
CFH [NCBI] 2.89067e-05
MEN1 [NCBI] 2.68486e-05
LSA [NCBI] 2.29957e-05
HGF [NCBI] 1.98873e-05
HP [NCBI] 1.7741e-05
ALB [NCBI] 1.61238e-05
ACH [NCBI] 1.50446e-05
BCNS [NCBI] 1.05775e-05
ADA [NCBI] 9.31392e-06
RNASE3 [NCBI] 8.87998e-06
CAT [NCBI] 6.5585e-06
MFS [NCBI] 6.15587e-06
AVP [NCBI] 3.62589e-06
thrombocytopenic purpura, autoimmune [NCBI] 3.1083e-06
VEGF [NCBI] 1.50931e-06
PRL [NCBI] 1.2807e-06
TNF [NCBI] 9.36158e-07
MG [NCBI] 2.06641e-07



Database Center for Life Science