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01 Ehlers-Danlos Syndrome [NCBI]


Gene


Gene Link Information
Gain
01
COL3A1 [NCBI] 0.000736912
TNXB [NCBI] 0.000253786
COL5A1 [NCBI] 0.000139716
PLOD1 [NCBI] 0.000136379
ADAMTS2 [NCBI] 9.7885e-05
COL1A2 [NCBI] 8.27925e-05
COL1A1 [NCBI] 7.82519e-05
COL5A2 [NCBI] 5.92028e-05
ADAMTS3 [NCBI] 5.10284e-05
ATP7A [NCBI] 4.50329e-05
SLC39A13 [NCBI] 4.441e-05
B4GALT7 [NCBI] 4.05478e-05
PLOD2 [NCBI] 3.28253e-05
DCN [NCBI] 2.57385e-05
ADAMTS14 [NCBI] 2.4835e-05
ADAMTS4 [NCBI] 1.84364e-05
FLNA [NCBI] 1.54068e-05
ADAMTS6 [NCBI] 1.4792e-05
COL5A3 [NCBI] 1.4792e-05
ADAMTS20 [NCBI] 1.4792e-05
ADAMTS7 [NCBI] 1.09305e-05
ADAMTS12 [NCBI] 1.09305e-05
ADAMTS10 [NCBI] 1.04969e-05
ARFGEF2 [NCBI] 1.04969e-05
ADAMTS9 [NCBI] 8.74193e-06
TGFBR1 [NCBI] 8.28423e-06
SLC2A10 [NCBI] 8.26624e-06
BGN [NCBI] 7.33128e-06
PITX2 [NCBI] 6.90889e-06
ADAMTS5 [NCBI] 6.86279e-06
ADAMTS1 [NCBI] 6.73156e-06
GSTT1 [NCBI] 6.13706e-06
TNC [NCBI] 6.04857e-06
PITX1 [NCBI] 6.04857e-06
PITX3 [NCBI] 5.8378e-06
GSTM1 [NCBI] 5.53558e-06
TGFBR2 [NCBI] 5.32946e-06
EDA [NCBI] 5.17281e-06
ABCC6 [NCBI] 5.06046e-06
IGFBP1 [NCBI] 4.48958e-06
ADAMTS13 [NCBI] 2.52612e-06
PTK2 [NCBI] 2.3895e-06
GSTP1 [NCBI] 1.65695e-06
TGFB1 [NCBI] 6.10885e-07




OMIM


OMIM Link Information
gain
01
ehlers-danlos syndrome, type viii [NCBI] 0.0100121
ehlers-danlos syndrome, type vib [NCBI] 0.00469457
ehlers-danlos syndrome, type i [NCBI] 0.00392288
ehlers-danlos syndrome, type iv, autosomal dominant [NCBI] 0.00339845
ehlers-danlos syndrome, type v [NCBI] 0.00290304
COL3A1 [NCBI] 0.00262154
ehlers-danlos syndrome, type vi [NCBI] 0.00184289
PLOD1 [NCBI] 0.00132792
ehlers-danlos syndrome, type vii, autosomal dominant [NCBI] 0.00122251
ehlers-danlos syndrome, type ii [NCBI] 0.00122251
COL1A2 [NCBI] 0.00115866
ehlers-danlos syndrome, type vii, autosomal recessive [NCBI] 0.000959149
cutis laxa, x-linked [NCBI] 0.000942306
COL5A1 [NCBI] 0.000810713
joint laxity, familial [NCBI] 0.000742078
ehlers-danlos syndrome, type iii [NCBI] 0.0006342
marfanoid hypermobility syndrome [NCBI] 0.0006095
dentin dysplasia, type i [NCBI] 0.000567689
heterotopia, periventricular, ehlers-danlos variant [NCBI] 0.00040595
TNXB [NCBI] 0.000338763
menkes disease [NCBI] 0.000319093
ehlers-danlos syndrome, autosomal recessive, cardiac valvular form [NCBI] 0.000304319
ehlers-danlos-like syndrome due to tenascin-x deficiency [NCBI] 0.000304319
COL1A1 [NCBI] 0.000286147
ATS [NCBI] 0.000276149
aneurysm, intracranial berry, 1 [NCBI] 0.000261717
ATP7A [NCBI] 0.000256904
ehlers-danlos syndrome, progeroid form [NCBI] 0.000249831
ehlers-danlos syndrome with platelet dysfunction from fibronectin abnormality [NCBI] 0.000202785
CF [NCBI] 0.000148872
cutis laxa, autosomal dominant [NCBI] 0.000107705
FLNA [NCBI] 0.000107126
COL5A2 [NCBI] 0.000106721
ehlers-danlos syndrome, autosomal dominant, type unspecified [NCBI] 0.000101345
ehlers-danlos syndrome, beasley-cohen type [NCBI] 0.000101345
osteogenesis imperfecta, type i [NCBI] 9.64572e-05
cutis laxa, autosomal recessive, type i [NCBI] 9.63133e-05
DCN [NCBI] 7.67367e-05
COL5A3 [NCBI] 7.00337e-05
ADAMTS14 [NCBI] 7.00337e-05
ADAMTS2 [NCBI] 7.00337e-05
furlong syndrome: fs [NCBI] 6.49753e-05
angioid streaks [NCBI] 6.09106e-05
B4GALT7 [NCBI] 5.62616e-05
ADAMTS1 [NCBI] 5.10688e-05
dentinogenesis imperfecta, shields type iii [NCBI] 4.89277e-05
WSS [NCBI] 4.58905e-05
LDS [NCBI] 4.45693e-05
xanthinuria, type i [NCBI] 4.11742e-05
DGI1 [NCBI] 4.11742e-05
osteoporosis, juvenile [NCBI] 4.01916e-05
TGFBR1 [NCBI] 3.8894e-05
EPS [NCBI] 3.60556e-05
UCMD [NCBI] 3.46759e-05
BGN [NCBI] 3.29783e-05
LCA1 [NCBI] 3.06672e-05
TGFBR2 [NCBI] 2.81147e-05
MFS [NCBI] 2.1454e-05
aortic valve disease [NCBI] 2.09821e-05
osteogenesis imperfecta, type iia [NCBI] 2.07385e-05
ELN [NCBI] 1.99851e-05
SVAS [NCBI] 1.61581e-05
HHT [NCBI] 1.47605e-05
PXE [NCBI] 4.16399e-06
polycystic kidneys [NCBI] 6.58793e-07




Database Center for Life Science