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MeSH keywords -> Related genes, diseases (OMIM)


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01 Klippel-Feil Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
KFM [NCBI] 0.000438875
FOP [NCBI] 0.000210575
PAX1 [NCBI] 4.70967e-05
GDF6 [NCBI] 1.58575e-05
NOG [NCBI] 1.02558e-05
FGFR3 [NCBI] 8.15578e-06



OMIM


 OMIM Link Information
gain		 01
klippel-feil syndrome, autosomal dominant [NCBI] 0.00800204
klippel-feil syndrome, autosomal recessive [NCBI] 0.00593937
SGM1 [NCBI] 0.0039217
sprengel deformity [NCBI] 0.00164346
wildervanck syndrome [NCBI] 0.00121496
poland syndrome [NCBI] 0.000757362
hemifacial microsomia with radial defects [NCBI] 0.000575485
gordon syndrome [NCBI] 0.000459383
pena-shokeir syndrome, type i [NCBI] 0.000245071
DWS [NCBI] 0.000241468
murcs association [NCBI] 0.000211037
PAX1 [NCBI] 0.000176026
muenke syndrome [NCBI] 8.87204e-05
SCDO1 [NCBI] 6.88341e-05
AMC [NCBI] 5.68389e-05
FOP [NCBI] 5.48607e-05
FGFR3 [NCBI] 4.52049e-05
FA [NCBI] 2.36081e-05



Database Center for Life Science