Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Ligaments [NCBI]

Gene


 Gene Link Information
Gain		 01
AIS [NCBI] 0.000282778
COMP [NCBI] 2.69661e-05
C1QTNF5 [NCBI] 2.55891e-05
INSL3 [NCBI] 2.17118e-05
GDF7 [NCBI] 1.50112e-05
BMP2 [NCBI] 1.33127e-05
MATN1 [NCBI] 1.30002e-05
FBN1 [NCBI] 1.07487e-05
ELN [NCBI] 1.07251e-05
GDF5 [NCBI] 1.05453e-05
TGFBI [NCBI] 8.86259e-06
NPY [NCBI] 8.72083e-06
GJB2 [NCBI] 7.29486e-06
MFRP [NCBI] 6.662e-06
TNMD [NCBI] 6.662e-06
GDF6 [NCBI] 6.4299e-06
COL12A1 [NCBI] 6.36314e-06
ACHE [NCBI] 6.25472e-06
FBN2 [NCBI] 6.24166e-06
TH [NCBI] 6.00239e-06
MSX2 [NCBI] 5.65357e-06
LECT1 [NCBI] 5.59201e-06
HOXA11 [NCBI] 5.47922e-06
TLE1 [NCBI] 5.42727e-06
SIX1 [NCBI] 5.30812e-06
FBLN5 [NCBI] 5.26418e-06
RLN2 [NCBI] 5.20169e-06
TNFAIP6 [NCBI] 5.08737e-06
GJB6 [NCBI] 5.03478e-06
POSTN [NCBI] 4.93726e-06
TNXB [NCBI] 4.83437e-06
SPARC [NCBI] 4.54554e-06
RYR1 [NCBI] 4.52487e-06
ZBTB16 [NCBI] 4.40913e-06
RUNX2 [NCBI] 3.72637e-06
HAPLN1 [NCBI] 3.66878e-06
PTH [NCBI] 3.2338e-06
MMP2 [NCBI] 3.10307e-06
BMP7 [NCBI] 2.91331e-06
NOG [NCBI] 2.73992e-06
PDGFA [NCBI] 2.72516e-06
ACP5 [NCBI] 2.2868e-06
TLR2 [NCBI] 2.21235e-06
CD68 [NCBI] 1.88414e-06
AR [NCBI] 1.41003e-06
GFAP [NCBI] 1.09887e-06
CDKN1A [NCBI] 9.74499e-07
PRL [NCBI] 9.11188e-07
NGF [NCBI] 6.47126e-07
TNF [NCBI] 3.23575e-07
EGF [NCBI] 2.84498e-07



OMIM


 OMIM Link Information
gain		 01
bruck syndrome 1 [NCBI] 0.00125871
cutis laxa, corneal clouding, and mental retardation [NCBI] 0.0012021
OPLL [NCBI] 0.000531796
IS1 [NCBI] 0.000475904
cutis laxa, autosomal recessive, type ii [NCBI] 0.000333314
spondylometaphyseal dysplasia with dentinogenesis imperfecta [NCBI] 0.000229418
costocoracoid ligament, congenitally short [NCBI] 0.000229418
celiac artery stenosis from compression by median arcuate ligament of diaphragm [NCBI] 0.000229418
bruck syndrome 2 [NCBI] 0.000190149
cryptorchidism, unilateral or bilateral [NCBI] 0.000158563
WSS [NCBI] 0.000148131
COMP [NCBI] 0.000145016
minicore myopathy with external ophthalmoplegia [NCBI] 0.000140535
hypophosphatemic rickets, x-linked dominant [NCBI] 0.000101871
CLS [NCBI] 9.09426e-05
INSL3 [NCBI] 6.55323e-05
WBS [NCBI] 6.19531e-05
SIX2 [NCBI] 5.24331e-05
SIX1 [NCBI] 3.70409e-05
RP [NCBI] 3.25133e-05
ZNF145 [NCBI] 2.84328e-05
FBN1 [NCBI] 2.64861e-05
RYR1 [NCBI] 2.59809e-05
NPY [NCBI] 2.58934e-05
BGLAP [NCBI] 1.9872e-05
ACHE [NCBI] 1.77184e-05
TLR2 [NCBI] 1.63161e-05
TH [NCBI] 1.60709e-05
AMH [NCBI] 1.54191e-05
RA [NCBI] 1.36135e-05
TTR [NCBI] 1.30152e-05
ACP5 [NCBI] 9.93858e-06
ADCYAP1 [NCBI] 9.03374e-06
PTH [NCBI] 6.47594e-06
AR [NCBI] 2.71292e-06
EGF [NCBI] 1.47838e-06
VEGF [NCBI] 9.02191e-07
GFAP [NCBI] 8.54318e-07
TNF [NCBI] 7.38842e-07
PRL [NCBI] 3.0388e-07
NGFB [NCBI] 4.48726e-09



Database Center for Life Science