Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hyperostosis	[NCBI]

Gene	Link	Information Gain
SOST	[NCBI]	7.16457e-05
FGF23	[NCBI]	2.77713e-05
FGFR3	[NCBI]	1.50307e-05
CTSH	[NCBI]	1.25575e-05
COL6A1	[NCBI]	1.12037e-05
ANKH	[NCBI]	1.05822e-05
ALPL	[NCBI]	9.741e-06
PHEX	[NCBI]	8.91372e-06
CTSL1	[NCBI]	6.22332e-06
ACP5	[NCBI]	5.90767e-06
STAT1	[NCBI]	5.83924e-06
TNFRSF11B	[NCBI]	5.49173e-06
TGFB1	[NCBI]	3.85559e-06
CDKN1A	[NCBI]	3.01271e-06

OMIM	Link	Information gain
proteus syndrome	[NCBI]	0.00215012
IH	[NCBI]	0.000697531
HHS	[NCBI]	0.000573952
SRS	[NCBI]	0.000328832
CDD	[NCBI]	0.00022125
lenz-majewski hyperostotic dwarfism	[NCBI]	0.000194697
SOST	[NCBI]	0.000170451
ectodermal dysplasia with natal teeth, turnpenny type	[NCBI]	0.000137445
hyperostosis cranialis interna	[NCBI]	0.000137445
BMND1	[NCBI]	9.36381e-05
FGFR3	[NCBI]	8.68024e-05
hyperostosis corticalis generalisata	[NCBI]	8.16836e-05
CMDD	[NCBI]	7.23386e-05
GALNT3	[NCBI]	6.83464e-05
SOST	[NCBI]	6.724e-05
MMP13	[NCBI]	6.724e-05
ANKH	[NCBI]	6.724e-05
CRMO	[NCBI]	5.39002e-05
FGF23	[NCBI]	5.08431e-05
TD1	[NCBI]	5.07618e-05
ACH	[NCBI]	4.39526e-05
BGLAP	[NCBI]	4.18653e-05
PTHLH	[NCBI]	2.7952e-05
APC	[NCBI]	1.06392e-05
VEGF	[NCBI]	3.92706e-06