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MeSH keywords -> Related genes, diseases (OMIM)


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01 Thanatophoric Dysplasia [NCBI]

Gene


 Gene Link Information
Gain		 01
FGFR3 [NCBI] 0.000702657
STAT1 [NCBI] 1.61031e-05
SOX9 [NCBI] 1.43814e-05
ARSE [NCBI] 9.79588e-06
SPRY2 [NCBI] 9.4021e-06
HSPG2 [NCBI] 9.15672e-06
IHH [NCBI] 9.08218e-06
LMAN1 [NCBI] 7.80634e-06
PTH1R [NCBI] 7.58015e-06
TYK2 [NCBI] 7.15413e-06
FGF3 [NCBI] 6.21903e-06
COL2A1 [NCBI] 5.84414e-06
FGF2 [NCBI] 5.74934e-06
MATN1 [NCBI] 4.7943e-06
ACHE [NCBI] 2.38288e-06
CDKN1A [NCBI] 9.73536e-07
PTH [NCBI] 8.05212e-07



OMIM


 OMIM Link Information
gain		 01
TD1 [NCBI] 0.00601148
FGFR3 [NCBI] 0.00210311
ACG1A [NCBI] 0.000661222
short rib-polydactyly syndrome, type ii [NCBI] 0.000650784
ATD1 [NCBI] 0.000521502
TD2 [NCBI] 0.000506787
micromelic bone dysplasia with cloverleaf skull [NCBI] 0.000354711
SRS [NCBI] 0.000328832
PLSDT [NCBI] 0.000287325
ACH [NCBI] 0.000256137
thanatophoric dysplasia, glasgow variant [NCBI] 0.000236205
schneckenbecken dysplasia [NCBI] 0.000168372
ACG2 [NCBI] 0.000143261
achondrogenesis, type iii [NCBI] 9.55083e-05
achondrogenesis, type iv [NCBI] 9.55083e-05
DDSH [NCBI] 8.154e-05
boomerang dysplasia [NCBI] 6.91863e-05
SLC35D1 [NCBI] 6.75778e-05
pseudotrisomy 13 syndrome [NCBI] 6.37593e-05
AOI [NCBI] 6.22947e-05
HSPG2 [NCBI] 5.0169e-05
HCH [NCBI] 4.47367e-05
SEDC [NCBI] 4.38454e-05
campomelic dysplasia [NCBI] 4.14448e-05
osteogenesis imperfecta, type iia [NCBI] 3.61793e-05
FGF2 [NCBI] 3.23729e-05
STAT1 [NCBI] 3.04786e-05
IHH [NCBI] 2.93032e-05
COL2A1 [NCBI] 2.85077e-05
ACHE [NCBI] 3.78241e-06
PTH [NCBI] 3.77539e-08



Database Center for Life Science