Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Femoral Fractures	[NCBI]

Gene	Link	Information Gain
BMP2	[NCBI]	9.54258e-05
BMP7	[NCBI]	4.1826e-05
ACP5	[NCBI]	1.83897e-05
PTH	[NCBI]	1.39253e-05
PCNA	[NCBI]	1.08816e-05
PTHLH	[NCBI]	9.59202e-06
WISP1	[NCBI]	9.50138e-06
CYP27B1	[NCBI]	8.8806e-06
TLR4	[NCBI]	8.84807e-06
BMPR1A	[NCBI]	8.56461e-06
DLX3	[NCBI]	8.42613e-06
ALPL	[NCBI]	8.04078e-06
CD68	[NCBI]	8.02904e-06
NOG	[NCBI]	6.6747e-06
BMPR2	[NCBI]	6.59355e-06
MGP	[NCBI]	6.46289e-06
COL1A1	[NCBI]	5.91348e-06
IGF2	[NCBI]	5.7008e-06
TNFRSF11A	[NCBI]	4.1047e-06
TNFSF11	[NCBI]	3.87311e-06
TNFRSF11B	[NCBI]	3.83228e-06
JAK2	[NCBI]	3.64264e-06
CALCA	[NCBI]	3.43028e-06
TGFB1	[NCBI]	2.26992e-06
MPO	[NCBI]	2.07796e-06
VEGFA	[NCBI]	2.00174e-06

OMIM	Link	Information gain
OSCS	[NCBI]	0.000807657
OD	[NCBI]	0.000727474
SPARC	[NCBI]	0.000107252
spinal muscular atrophy, type i, with congenital bone fractures	[NCBI]	0.000106079
IHH	[NCBI]	8.8358e-05
hypophosphatasia, adult type	[NCBI]	8.3156e-05
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant	[NCBI]	7.73439e-05
ABS	[NCBI]	7.56107e-05
SEDC	[NCBI]	7.21716e-05
CYP27B1	[NCBI]	5.33506e-05
MAS	[NCBI]	5.29633e-05
PTH	[NCBI]	5.11145e-05
SPP1	[NCBI]	4.58198e-05
PCNA	[NCBI]	4.00773e-05
ABP1	[NCBI]	3.23069e-05
RA	[NCBI]	2.24023e-05
TLR4	[NCBI]	2.12562e-05
ACP5	[NCBI]	2.04634e-05
PTHLH	[NCBI]	1.79607e-05
thrombocytopenic purpura, autoimmune	[NCBI]	1.75176e-05
TNFRSF11B	[NCBI]	1.61064e-05
MPO	[NCBI]	5.23793e-06
VEGF	[NCBI]	1.07227e-10