Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Exostoses, Multiple Hereditary [NCBI]

Gene


 Gene Link Information
Gain		 01
EXT3 [NCBI] 0.000817003
EXT1 [NCBI] 0.000485101
EXT2 [NCBI] 0.000463438
EXTL2P [NCBI] 0.000401057
PSS [NCBI] 0.000317391
EXTL3 [NCBI] 0.000149512
EXTL2 [NCBI] 8.51854e-05
EXTL1 [NCBI] 5.50567e-05
COL10A1 [NCBI] 4.41008e-05
PTHLH [NCBI] 4.0982e-05
ALX4 [NCBI] 3.29035e-05
SLC26A2 [NCBI] 2.69744e-05
SDC2 [NCBI] 1.82371e-05
FGFR3 [NCBI] 1.61241e-05
GALNT5 [NCBI] 1.57857e-05
CHSY1 [NCBI] 1.2507e-05
TRAP1 [NCBI] 1.06111e-05
PTH [NCBI] 9.65795e-06
HOXC8 [NCBI] 9.60189e-06
MATN3 [NCBI] 9.60189e-06
NCAN [NCBI] 8.38226e-06
SDC4 [NCBI] 8.09624e-06
GRPR [NCBI] 7.85136e-06
HAPLN1 [NCBI] 7.00602e-06
FGF4 [NCBI] 6.10312e-06
ILK [NCBI] 5.93317e-06
VCAN [NCBI] 5.46241e-06
COL2A1 [NCBI] 5.41864e-06
COMP [NCBI] 5.02621e-06
IBSP [NCBI] 5.01771e-06
BMP4 [NCBI] 4.79599e-06
CD44 [NCBI] 4.58761e-06
MATN1 [NCBI] 4.37405e-06
MMP13 [NCBI] 4.24764e-06
SHH [NCBI] 4.1552e-06
BMP2 [NCBI] 3.30393e-06
NOS2 [NCBI] 1.68726e-06



OMIM


 OMIM Link Information
gain		 01
exostoses, multiple, type i [NCBI] 0.00308126
EXT3 [NCBI] 0.00167995
exostoses, multiple, type ii [NCBI] 0.00163781
EXT1 [NCBI] 0.00140587
TRPS2 [NCBI] 0.00135355
upington disease [NCBI] 0.00105062
metaphyseal dysplasia, braun-tinschert type [NCBI] 0.00105062
EXT2 [NCBI] 0.00104929
metaphyseal acroscyphodysplasia [NCBI] 0.000832846
potocki-shaffer syndrome [NCBI] 0.000629905
fibrochondrogenesis [NCBI] 0.000626524
acrodysostosis [NCBI] 0.000558521
DBQD [NCBI] 0.00051152
OSCS [NCBI] 0.000486675
microcephalic osteodysplastic primordial dwarfism, type i [NCBI] 0.000455679
metachondromatosis [NCBI] 0.00044865
CGF [NCBI] 0.000446614
myeloproliferative syndrome, transient [NCBI] 0.000356832
EXTL1 [NCBI] 0.000238087
EXTL3 [NCBI] 0.000158523
EXTL2 [NCBI] 0.000158523
heat-shock protein, 75-kd [NCBI] 0.000139544
CHH [NCBI] 0.000135146
ALX4 [NCBI] 0.000116909
TRPS1 [NCBI] 0.000114141
polyposis, intestinal, with multiple exostoses [NCBI] 0.000111888
multiple exostoses with spastic tetraparesis [NCBI] 0.000111888
kniest-like dysplasia, lethal [NCBI] 0.000111888
metaphyseal chondrodysplasia, kaitila type [NCBI] 0.000111888
exostoses with anetodermia and brachydactyly, type e [NCBI] 0.000111888
eiken skeletal dysplasia [NCBI] 8.94311e-05
metaphyseal chondrodysplasia, spahr type [NCBI] 8.94311e-05
COL10A1 [NCBI] 8.69882e-05
chondrosarcoma [NCBI] 8.09651e-05
dysplasia epiphysealis hemimelica [NCBI] 8.09651e-05
TD1 [NCBI] 7.3995e-05
IHH [NCBI] 6.81885e-05
tibial hemimelia [NCBI] 6.81454e-05
COL2A1 [NCBI] 6.65735e-05
congenital disorder of glycosylation, type i/iix [NCBI] 6.54472e-05
schneckenbecken dysplasia [NCBI] 6.54472e-05
HOXC8 [NCBI] 6.53848e-05
SOX5 [NCBI] 6.53848e-05
TD2 [NCBI] 6.31397e-05
CDG2A [NCBI] 6.11243e-05
metaphyseal chondrodysplasia, jansen type [NCBI] 6.11243e-05
AOII [NCBI] 6.11243e-05
OGD [NCBI] 6.11243e-05
SOX6 [NCBI] 6.01867e-05
CDG1B [NCBI] 5.93356e-05
wagr syndrome [NCBI] 5.62685e-05
FRA16A [NCBI] 5.49323e-05
pulmonary alveolar microlithiasis [NCBI] 5.37003e-05
SDC2 [NCBI] 5.34339e-05
sacral defect with anterior meningocele [NCBI] 4.95569e-05
MATN3 [NCBI] 4.92232e-05
MMP13 [NCBI] 4.68774e-05
diastrophic dysplasia [NCBI] 4.35826e-05
SLC26A2 [NCBI] 4.26884e-05
PTHR1 [NCBI] 3.8347e-05
GRPR [NCBI] 3.79181e-05
CDG1A [NCBI] 3.35334e-05
MTS [NCBI] 2.87088e-05
PSORS1 [NCBI] 2.5655e-05
ALS1 [NCBI] 2.5655e-05
CCD [NCBI] 2.51177e-05
SDS [NCBI] 2.4103e-05
ILK [NCBI] 2.36408e-05
AHO [NCBI] 2.27123e-05
ACH [NCBI] 1.99491e-05
COMP [NCBI] 1.77854e-05
PTH [NCBI] 1.74927e-05
FGFR3 [NCBI] 1.60097e-05
NF1 [NCBI] 1.28253e-05
MFS [NCBI] 1.01506e-05



Database Center for Life Science