Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Clavicle [NCBI]

Gene


 Gene Link Information
Gain		 01
ZMPSTE24 [NCBI] 1.62227e-05
RUNX2 [NCBI] 1.1729e-05
BMP7 [NCBI] 1.008e-05
MSX2 [NCBI] 7.06649e-06
ATF1 [NCBI] 6.48168e-06
BMPR1B [NCBI] 6.44686e-06
ACVR1 [NCBI] 6.33375e-06
EWSR1 [NCBI] 6.30366e-06
BMPR1A [NCBI] 6.26014e-06
PAX1 [NCBI] 5.81962e-06
PIP [NCBI] 5.81052e-06
BMPR2 [NCBI] 5.6365e-06
ATP7A [NCBI] 5.59919e-06
SMAD1 [NCBI] 5.29793e-06
LMNA [NCBI] 5.06256e-06
KRT7 [NCBI] 5.01657e-06
FGF7 [NCBI] 4.48966e-06
BMP4 [NCBI] 4.18892e-06
BMP2 [NCBI] 3.32708e-06
AFP [NCBI] 3.2865e-06
PTH [NCBI] 2.28779e-06



OMIM


 OMIM Link Information
gain		 01
microcephalic osteodysplastic primordial dwarfism, type iii [NCBI] 0.00145218
microcephalic osteodysplastic primordial dwarfism, type i [NCBI] 0.00131934
kabuki syndrome [NCBI] 0.000816485
CCD [NCBI] 0.000764697
CRMO [NCBI] 0.000515369
MADA [NCBI] 0.000421156
genochondromatosis [NCBI] 0.000218857
clavicular hypoplasia, zygomatic arch hypoplasia, and micrognathia [NCBI] 0.000218857
costocoracoid ligament, congenitally short [NCBI] 0.000218857
cleidorhizomelic syndrome [NCBI] 0.000218857
PFMCCD [NCBI] 0.000218857
pelvis-shoulder dysplasia [NCBI] 0.000155164
MADB [NCBI] 0.000155164
floating-harbor syndrome [NCBI] 0.000142325
RNS [NCBI] 0.000130005
camurati-engelmann disease [NCBI] 0.000114936
PFM [NCBI] 0.000102582
AHO [NCBI] 7.89418e-05
MAS [NCBI] 7.28327e-05
F7R [NCBI] 5.64253e-05
FAM20C [NCBI] 5.49754e-05
ALX4 [NCBI] 5.27376e-05
ZMPSTE24 [NCBI] 5.27376e-05
MSX2 [NCBI] 5.03125e-05
LMNA [NCBI] 3.67117e-05
AFP [NCBI] 1.55712e-05
PTH [NCBI] 8.72299e-06



Database Center for Life Science