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01 Osteogenesis Imperfecta [NCBI]

Gene


 Gene Link Information
Gain		 01
COL1A1 [NCBI] 0.00102162
COL1A2 [NCBI] 0.000621129
CRTAP [NCBI] 5.97557e-05
LEPRE1 [NCBI] 4.09361e-05
PPIB [NCBI] 1.72437e-05
ADAMTS2 [NCBI] 1.40389e-05
BMP2 [NCBI] 1.2889e-05
PLOD2 [NCBI] 9.01319e-06
ARSE [NCBI] 8.50154e-06
SFRS2 [NCBI] 7.78906e-06
PTH [NCBI] 6.60483e-06
LOX [NCBI] 6.41703e-06
LRP5 [NCBI] 6.3534e-06
EDA [NCBI] 5.2991e-06
ESD [NCBI] 5.12558e-06
COL2A1 [NCBI] 4.57142e-06
COMP [NCBI] 4.18368e-06
IBSP [NCBI] 4.17529e-06
GNAS [NCBI] 4.10174e-06
FGFR3 [NCBI] 2.71251e-06
CTGF [NCBI] 2.36487e-06
TNFRSF11B [NCBI] 1.99974e-06
PTHLH [NCBI] 1.81391e-06
VDR [NCBI] 1.64061e-06
CFTR [NCBI] 2.94421e-07



OMIM


 OMIM Link Information
gain		 01
osteogenesis imperfecta, type i [NCBI] 0.0077687
osteogenesis imperfecta, type iia [NCBI] 0.00575407
COL1A1 [NCBI] 0.00490683
COL1A2 [NCBI] 0.00321943
osteogenesis imperfecta, type v [NCBI] 0.00311346
osteogenesis imperfecta, type vi [NCBI] 0.00311346
bruck syndrome 1 [NCBI] 0.00258477
osteogenesis imperfecta, type iii [NCBI] 0.00213225
osteogenesis imperfecta, type iv [NCBI] 0.00183221
ehlers-danlos syndrome, type vib [NCBI] 0.00124472
joint laxity, familial [NCBI] 0.000807657
dentin dysplasia, type i [NCBI] 0.000632907
metatropic dwarfism [NCBI] 0.000575369
osteoporosis, juvenile [NCBI] 0.000508781
OPPG [NCBI] 0.000508781
osteogenesis imperfecta, type viii [NCBI] 0.000496109
ACG1A [NCBI] 0.000450881
osteogenesis imperfecta, type vii [NCBI] 0.000396721
ATD1 [NCBI] 0.000314772
bone fragility with craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features [NCBI] 0.000297417
osteogenesis imperfecta, type iib [NCBI] 0.000297417
LEPRE1 [NCBI] 0.000253281
CRTAP [NCBI] 0.000208495
osteogenesis imperfecta with opalescent teeth [NCBI] 0.000198196
TD1 [NCBI] 0.000142768
GDD [NCBI] 0.000125484
SMPD3 [NCBI] 0.000119949
DGI1 [NCBI] 0.000100973
osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones, but without fractures [NCBI] 9.90568e-05
grant syndrome [NCBI] 9.90568e-05
osteopenia and sparse hair [NCBI] 9.90568e-05
cortical defects, wormian bones, and dentinogenesis imperfecta [NCBI] 9.90568e-05
prenatal bowing [NCBI] 9.90568e-05
sella turcica, bridged [NCBI] 9.90568e-05
osteogenesis imperfecta, sillence type ii/iii, without abnormality of type i collagen [NCBI] 9.90568e-05
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant [NCBI] 8.35173e-05
arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly [NCBI] 7.662e-05
thanatophoric dysplasia, glasgow variant [NCBI] 7.662e-05
gracile bone dysplasia [NCBI] 5.54132e-05
COL2A1 [NCBI] 4.74049e-05
dentinogenesis imperfecta, shields type iii [NCBI] 4.66822e-05
ehlers-danlos syndrome, type vii, autosomal dominant [NCBI] 4.36545e-05
PPIB [NCBI] 4.25966e-05
ACG2 [NCBI] 4.11257e-05
caffey disease [NCBI] 4.00028e-05
ehlers-danlos syndrome, type vii, autosomal recessive [NCBI] 3.89572e-05
pycnodysostosis [NCBI] 3.70611e-05
hypophosphatasia, adult type [NCBI] 3.6196e-05
EPS [NCBI] 3.38671e-05
DCN [NCBI] 3.06452e-05
ehlers-danlos syndrome, type i [NCBI] 2.54233e-05
contractural arachnodactyly, congenital [NCBI] 2.40545e-05
mucolipidosis ii [NCBI] 1.97148e-05
FRDA [NCBI] 9.88773e-06
ACH [NCBI] 9.48437e-06
COMP [NCBI] 9.13053e-06
ACP5 [NCBI] 3.81453e-06
MFS [NCBI] 2.27247e-06
VDR [NCBI] 4.40009e-07
PTH [NCBI] 2.37923e-07
polycystic kidneys [NCBI] 1.92111e-07



Database Center for Life Science