Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Fibrous Dysplasia, Polyostotic	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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