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MeSH keywords -> Related genes, diseases (OMIM)


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01 Muscular Dystrophy, Facioscapulohumeral [NCBI]

Gene


 Gene Link Information
Gain		 01
FSHMD1A [NCBI] 0.00190856
FSHMD1B [NCBI] 0.000297502
FRG1 [NCBI] 0.000142624
FRG2 [NCBI] 8.96742e-05
DUX4 [NCBI] 8.05862e-05
TUBB4Q [NCBI] 3.56605e-05
FRG2B [NCBI] 3.56605e-05
SLC25A4 [NCBI] 2.32897e-05
MYOD1 [NCBI] 1.78702e-05
SYCE1 [NCBI] 1.77972e-05
FRG2C [NCBI] 1.54168e-05
RP11-631M21.2 [NCBI] 1.54168e-05
LOC441056 [NCBI] 1.45183e-05
LOC653543 [NCBI] 1.45183e-05
LOC653548 [NCBI] 1.45183e-05
LOC653541 [NCBI] 1.45183e-05
LOC728410 [NCBI] 1.45183e-05
LOC653544 [NCBI] 1.45183e-05
LOC653545 [NCBI] 1.45183e-05
CRYM [NCBI] 1.31553e-05
TNNT3 [NCBI] 1.28678e-05
NCL [NCBI] 1.09805e-05
FXR1 [NCBI] 1.03293e-05
YY1 [NCBI] 9.24908e-06
PITX1 [NCBI] 9.0383e-06
FGFR4 [NCBI] 8.57032e-06
AQP4 [NCBI] 8.22081e-06
BAX [NCBI] 3.03806e-06
CASP3 [NCBI] 2.43221e-06



OMIM


 OMIM Link Information
gain		 01
FSHMD1A [NCBI] 0.0239578
FSHMD1B [NCBI] 0.000665076
fshd gene 2 [NCBI] 0.00029456
FRG1 [NCBI] 0.0002722
coats disease [NCBI] 0.00012944
immunodeficiency-centromeric instability-facial anomalies syndrome [NCBI] 9.68753e-05
DUX4 [NCBI] 8.31009e-05
NCL [NCBI] 7.79e-05
leber optic atrophy [NCBI] 6.91855e-05
SLC25A4 [NCBI] 5.64542e-05
MTND4 [NCBI] 4.72252e-05
AGER [NCBI] 3.85868e-05
SDC2 [NCBI] 3.7246e-05



Database Center for Life Science