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01 Fibrous Dysplasia, Polyostotic [NCBI]

Gene


 Gene Link Information
Gain		 01
GNAS [NCBI] 0.000818851
BDMR [NCBI] 0.000438875
FOP [NCBI] 0.000210575
FGF23 [NCBI] 7.5198e-05
PTH [NCBI] 2.88024e-05
GPC1 [NCBI] 2.20913e-05
ALMS1 [NCBI] 1.93056e-05
PHEX [NCBI] 1.46864e-05
GNG4 [NCBI] 1.25476e-05
GNG3 [NCBI] 1.19643e-05
GNB5 [NCBI] 1.19643e-05
GNB4 [NCBI] 1.19643e-05
GNG11 [NCBI] 1.15306e-05
GPR35 [NCBI] 1.15306e-05
DBNL [NCBI] 1.1185e-05
GNB2 [NCBI] 1.1185e-05
GNAI3 [NCBI] 1.1185e-05
GNB1 [NCBI] 1.06517e-05
DIO1 [NCBI] 1.02456e-05
GNA13 [NCBI] 1.00738e-05
FGD1 [NCBI] 8.42279e-06
DIO2 [NCBI] 6.83778e-06
CTTN [NCBI] 6.60863e-06
KAL1 [NCBI] 6.20969e-06
PRKAR1A [NCBI] 5.7924e-06
NF1 [NCBI] 5.6172e-06
GNB3 [NCBI] 5.42656e-06
BMP4 [NCBI] 4.83571e-06
MEN1 [NCBI] 3.90306e-06
BMP2 [NCBI] 3.34229e-06
CD68 [NCBI] 1.90034e-06
CFTR [NCBI] 8.32295e-07



OMIM


 OMIM Link Information
gain		 01
MAS [NCBI] 0.010553
brachydactyly-mental retardation syndrome [NCBI] 0.00390348
AHO [NCBI] 0.00179507
GNAS [NCBI] 0.00163802
GPC1 [NCBI] 0.000163464
STK25 [NCBI] 8.16043e-05
PTH [NCBI] 7.69911e-05
GNRH1 [NCBI] 7.56807e-05
BDE [NCBI] 5.78337e-05
GDD [NCBI] 5.78337e-05
osseous heteroplasia, progressive [NCBI] 5.58247e-05
TFAP2C [NCBI] 5.30825e-05
sturge-weber syndrome [NCBI] 5.24412e-05
oculocerebrocutaneous syndrome [NCBI] 5.09881e-05
FGD1 [NCBI] 4.93128e-05
pseudohypoparathyroidism, type ib [NCBI] 4.43148e-05
NKX2E [NCBI] 4.21875e-05
PTHLH [NCBI] 3.49609e-05
AIMAH [NCBI] 3.12307e-05
FOP [NCBI] 2.15469e-05



Database Center for Life Science