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MeSH keywords -> Related genes, diseases (OMIM)


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01 Femoral Fractures [NCBI]


Gene


Gene Link Information
Gain
01
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


OMIM Link Information
gain
01
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




Database Center for Life Science