Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Frontal Bone [NCBI]

Gene


 Gene Link Information
Gain		 01
FND [NCBI] 0.000442596
FGFR3 [NCBI] 3.86854e-05
TWIST1 [NCBI] 1.2282e-05
BMP2 [NCBI] 7.83474e-06
MSX1 [NCBI] 7.0373e-06
MSX2 [NCBI] 6.93711e-06
CSTB [NCBI] 6.13081e-06
NQO1 [NCBI] 5.03703e-06
CDK5 [NCBI] 4.28003e-06
NOG [NCBI] 4.00672e-06
TGFBR1 [NCBI] 3.95431e-06
ACP5 [NCBI] 3.54308e-06



OMIM


 OMIM Link Information
gain		 01
hypertelorism, teebi type [NCBI] 0.00112601
CMDR [NCBI] 0.00102443
PCA [NCBI] 0.000859563
OSCS [NCBI] 0.000859563
HFM [NCBI] 0.000516497
FMD [NCBI] 0.000298145
CFNS [NCBI] 0.000265855
craniotelencephalic dysplasia [NCBI] 0.000175333
monosomy 9p syndrome [NCBI] 0.000158563
iris coloboma with ptosis, hypertelorism, and mental retardation [NCBI] 0.000158563
frontonasal dysplasia [NCBI] 0.000140535
crouzon syndrome [NCBI] 0.000140535
heterotopia, periventricular, x-linked dominant [NCBI] 0.000125443
mulibrey nanism [NCBI] 0.000125443
apert syndrome [NCBI] 0.000125443
MNS [NCBI] 0.000117088
GCPS [NCBI] 9.87087e-05
APC [NCBI] 9.76924e-05
CRMO [NCBI] 9.72532e-05
FGFR3 [NCBI] 8.96306e-05
ACP5 [NCBI] 2.82046e-05
CJD [NCBI] 2.57713e-05



Database Center for Life Science