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01 Pelvic Bones [NCBI]

Gene


 Gene Link Information
Gain		 01
ATD [NCBI] 0.000510938
PTH [NCBI] 2.27127e-05
PITX1 [NCBI] 1.14053e-05
PLCL1 [NCBI] 8.87523e-06
TBX4 [NCBI] 7.8725e-06
HYAL1 [NCBI] 7.20492e-06
COL10A1 [NCBI] 7.20492e-06
LCT [NCBI] 6.9654e-06
FBLN5 [NCBI] 6.28232e-06
NDP [NCBI] 6.142e-06
NR4A3 [NCBI] 6.00257e-06
PAX1 [NCBI] 5.42561e-06
FGFR3 [NCBI] 4.21426e-06
ATM [NCBI] 4.12391e-06
IGF1 [NCBI] 4.06874e-06
BMP7 [NCBI] 3.91959e-06
VDR [NCBI] 3.2473e-06
TNF [NCBI] 1.09003e-06



OMIM


 OMIM Link Information
gain		 01
ATD1 [NCBI] 0.00394655
spondylometaphyseal dysplasia, kozlowski type [NCBI] 0.00232265
bone size quantitative trait locus 3 [NCBI] 0.00136729
upington disease [NCBI] 0.00136729
microcephalic osteodysplastic primordial dwarfism, type iii [NCBI] 0.000939888
bone size quantitative trait locus 1 [NCBI] 0.000939888
spondyloepiphyseal dysplasia tarda, autosomal dominant [NCBI] 0.000939888
microcephalic osteodysplastic primordial dwarfism, type i [NCBI] 0.000807956
ulna and fibula, absence of, with severe limb deficiency [NCBI] 0.000751854
BMND3 [NCBI] 0.000726199
hypertension with brachydactyly [NCBI] 0.000694531
proteus syndrome [NCBI] 0.000475184
SPS [NCBI] 0.000460573
klippel-trenaunay-weber syndrome [NCBI] 0.000359351
HCH [NCBI] 0.000339304
osteomesopyknosis [NCBI] 0.000330968
spondyloepimetaphyseal dysplasia, strudwick type [NCBI] 0.000243512
CCD [NCBI] 0.000234475
FFS [NCBI] 0.000232164
sao paulo mca/mr syndrome [NCBI] 0.000192271
eiken skeletal dysplasia [NCBI] 0.000192271
acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia [NCBI] 0.000153026
aneurysmal bone cysts [NCBI] 0.000153026
hyaluronidase deficiency [NCBI] 0.000153026
pelvic hypoplasia with lower-limb arthrogryposis [NCBI] 0.000153026
thoracopelvic dysostosis [NCBI] 0.000153026
hyaluronan metabolism, defect in [NCBI] 0.000153026
ulna metaphyseal dysplasia syndrome [NCBI] 0.000153026
ankylosing vertebral hyperostosis with tylosis [NCBI] 0.000138233
OPTA1 [NCBI] 0.000138233
gurrieri syndrome [NCBI] 0.000138233
ACH [NCBI] 0.000131453
TLPD [NCBI] 0.000128637
growth-mental deficiency syndrome of myhre [NCBI] 0.000115837
avascular necrosis of femoral head, primary [NCBI] 0.000115837
fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly [NCBI] 0.000115837
OSMED [NCBI] 0.000115837
MCDS [NCBI] 0.000115837
pituitary dwarfism i [NCBI] 0.000115837
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus [NCBI] 0.000111124
OPTA2 [NCBI] 0.000111124
pycnodysostosis [NCBI] 0.000103575
alkaptonuria [NCBI] 0.000100453
paget disease, juvenile [NCBI] 9.50988e-05
FMD [NCBI] 9.0617e-05
camurati-engelmann disease [NCBI] 8.86232e-05
PTH [NCBI] 8.51463e-05
SLSN1 [NCBI] 8.50245e-05
mucolipidosis iiia [NCBI] 8.33887e-05
HFTC [NCBI] 8.03855e-05
PPS [NCBI] 7.9e-05
hypophosphatasia, infantile [NCBI] 7.9e-05
mucopolysaccharidosis type vi [NCBI] 7.7682e-05
mucopolysaccharidosis type vii [NCBI] 7.64255e-05
CFNS [NCBI] 7.5225e-05
EVC [NCBI] 7.2974e-05
BMD [NCBI] 6.63232e-05
HYAL1 [NCBI] 5.41316e-05
PSACH [NCBI] 5.33702e-05
TBX4 [NCBI] 4.96571e-05
COL10A1 [NCBI] 4.38763e-05
PTHR1 [NCBI] 3.95374e-05
SLE [NCBI] 3.67128e-05
GUSB [NCBI] 3.03319e-05
FMF [NCBI] 2.08962e-05
VDR [NCBI] 1.45069e-05
KLK3 [NCBI] 1.09268e-05



Database Center for Life Science