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MeSH keywords -> Related genes, diseases (OMIM)


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01 Achondroplasia [NCBI]

Gene


 Gene Link Information
Gain		 01
FGFR3 [NCBI] 0.00140506
MATN1 [NCBI] 0.00041941
COMP [NCBI] 0.000400912
COL2A1 [NCBI] 4.29704e-05
SLC26A2 [NCBI] 4.26544e-05
IHH [NCBI] 1.70344e-05
FGF3 [NCBI] 1.12589e-05
BMP8B [NCBI] 1.01242e-05
PTHLH [NCBI] 9.2042e-06
NPR2 [NCBI] 8.66864e-06
ARSE [NCBI] 8.00144e-06
PTH1R [NCBI] 5.79602e-06
HAPLN1 [NCBI] 5.65234e-06
SHOX [NCBI] 4.4656e-06
SOX9 [NCBI] 4.22905e-06
FGF2 [NCBI] 3.99262e-06
BMP4 [NCBI] 3.47738e-06
PAX3 [NCBI] 3.42087e-06
SNAI2 [NCBI] 3.33325e-06
MAP2K1 [NCBI] 3.06378e-06
PKD1 [NCBI] 2.35944e-06
STAT1 [NCBI] 1.87089e-06
EPO [NCBI] 2.98852e-07
CFTR [NCBI] 9.73067e-08
PTH [NCBI] 9.3262e-09



OMIM


 OMIM Link Information
gain		 01
ACH [NCBI] 0.0103574
ACG1A [NCBI] 0.00746644
PSACH [NCBI] 0.00461046
FGFR3 [NCBI] 0.00379016
ATD1 [NCBI] 0.00195608
HCH [NCBI] 0.00180644
COMP [NCBI] 0.00174245
metatropic dwarfism [NCBI] 0.00128649
spondyloenchondrodysplasia [NCBI] 0.00106928
TD1 [NCBI] 0.000786895
ACG2 [NCBI] 0.000532395
dyssegmental dysplasia, rolland-desbuquois type [NCBI] 0.000495941
acrodysostosis [NCBI] 0.000476563
short rib-polydactyly syndrome, type ii [NCBI] 0.000384327
robinow syndrome, autosomal dominant [NCBI] 0.00035748
SEDC [NCBI] 0.000255713
EDM1 [NCBI] 0.000164094
acromesomelic dysplasia, hunter-thompson type [NCBI] 0.000119572
AMDM [NCBI] 0.000112381
baby rattle pelvis dysplasia [NCBI] 9.82561e-05
CHH [NCBI] 9.54247e-05
IHH [NCBI] 8.8807e-05
COL2A1 [NCBI] 8.63857e-05
kleeblattschaedel syndrome [NCBI] 7.58211e-05
achondrogenesis, type iv [NCBI] 7.58211e-05
achondrogenesis, type iii [NCBI] 7.58211e-05
pyknoachondrogenesis [NCBI] 7.58211e-05
metaphyseal chondrodysplasia, spahr type [NCBI] 7.58211e-05
camptodactyly, tall stature, and hearing loss syndrome [NCBI] 7.58211e-05
BMP8 [NCBI] 7.05168e-05
peripheral dysostosis [NCBI] 6.73767e-05
ACG1B [NCBI] 6.19061e-05
TLPD [NCBI] 6.19061e-05
NPPC [NCBI] 5.67442e-05
achondroplasia, so-called, and severe combined immunodeficiency [NCBI] 5.19449e-05
schneckenbecken dysplasia [NCBI] 5.19449e-05
boomerang dysplasia [NCBI] 4.96589e-05
chondrodysplasia, grebe type [NCBI] 4.58979e-05
EVC [NCBI] 4.56779e-05
NPR2 [NCBI] 4.56779e-05
AOI [NCBI] 4.28739e-05
AGC1 [NCBI] 4.20282e-05
PAPSS2 [NCBI] 4.06114e-05
kniest dysplasia [NCBI] 3.92276e-05
PABPN1 [NCBI] 3.72877e-05
pycnodysostosis [NCBI] 3.62915e-05
MCDS [NCBI] 3.54282e-05
SLC26A2 [NCBI] 3.41102e-05
PTHR1 [NCBI] 2.98072e-05
IGF1 [NCBI] 2.62336e-05
EVC [NCBI] 2.43013e-05
ehlers-danlos syndrome, type iv, autosomal dominant [NCBI] 2.43013e-05
exostoses, multiple, type i [NCBI] 2.39234e-05
NF1 [NCBI] 2.267e-05
FGF2 [NCBI] 2.18135e-05
LWD [NCBI] 2.15428e-05
osteogenesis imperfecta, type iia [NCBI] 1.80374e-05
PTHLH [NCBI] 1.54108e-05
CCD [NCBI] 1.32955e-05
FGFR2 [NCBI] 1.29534e-05
PTH [NCBI] 1.06035e-05
EPO [NCBI] 2.52659e-06
dystrophia myotonica 1 [NCBI] 2.42172e-06
MFS [NCBI] 1.93067e-06
SPP1 [NCBI] 1.80822e-06
HD [NCBI] 1.51169e-06



Database Center for Life Science