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MeSH keywords -> Related genes, diseases (OMIM)


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01 Muscular Dystrophies, Limb-Girdle [NCBI]


Gene


Gene Link Information
Gain
01
CAPN3 [NCBI] 0.000430781
LGMD1G [NCBI] 0.000415947
LGMD2L [NCBI] 0.000415947
DYSF [NCBI] 0.0003683
LGMD1F [NCBI] 0.000355204
FKRP [NCBI] 0.000242791
LMNA [NCBI] 6.93481e-05
CAV3 [NCBI] 6.90972e-05
TRIM32 [NCBI] 4.50325e-05
MYOT [NCBI] 2.76159e-05
FKTN [NCBI] 2.4399e-05
POMT2 [NCBI] 2.30225e-05
DOK7 [NCBI] 2.20279e-05
POMT1 [NCBI] 2.06314e-05
SGCG [NCBI] 1.94345e-05
SGCB [NCBI] 1.88766e-05
FBXO40 [NCBI] 1.50995e-05
SPATA18 [NCBI] 1.50995e-05
AQP4 [NCBI] 1.34723e-05
MSTN [NCBI] 1.29221e-05
SYTL2 [NCBI] 1.12378e-05
AHNAK [NCBI] 1.08041e-05
MYOF [NCBI] 1.01714e-05
PDLIM3 [NCBI] 1.01714e-05
COL6A3 [NCBI] 9.19178e-06
POMGNT1 [NCBI] 8.79431e-06
PIAS4 [NCBI] 8.68001e-06
UBE2N [NCBI] 8.57288e-06
VCL [NCBI] 8.37688e-06
DTNA [NCBI] 8.37688e-06
LARGE [NCBI] 8.37688e-06
MAN1C1 [NCBI] 8.28672e-06
NFKB1 [NCBI] 7.99073e-06
IL32 [NCBI] 7.89599e-06
TCAP [NCBI] 7.89599e-06
XK [NCBI] 7.63731e-06
EMD [NCBI] 7.36102e-06
FRZB [NCBI] 6.91504e-06
CSRP3 [NCBI] 6.76501e-06
RAB27A [NCBI] 6.69471e-06
AQP1 [NCBI] 6.59444e-06
VCP [NCBI] 6.4998e-06
RAGE [NCBI] 5.93214e-06
MYOD1 [NCBI] 5.03823e-06
AGER [NCBI] 4.96318e-06
DAG1 [NCBI] 3.9891e-06
DDIT3 [NCBI] 3.98241e-06
CFLAR [NCBI] 3.33917e-06
PMP22 [NCBI] 3.12484e-06
PLN [NCBI] 3.09817e-06
VDR [NCBI] 1.79111e-06
AKT1 [NCBI] 1.06189e-06




OMIM


OMIM Link Information
gain
01
LGMD1G [NCBI] 0.00129156
LGMD2L [NCBI] 0.00107364
myopathy, limb-girdle, with bone fragility [NCBI] 0.00107364
diaphyseal medullary stenosis with malignant fibrous histiocytoma [NCBI] 0.000938013
CAPN3 [NCBI] 0.00073807
LGMD2I [NCBI] 0.000672013
LGMD2A [NCBI] 0.000665899
FKRP [NCBI] 0.000359592
LGMD2H [NCBI] 0.00030606
DYSF [NCBI] 0.000283225
TRIM32 [NCBI] 0.000203128
MM [NCBI] 0.000141541
LGMD2M [NCBI] 0.000134271
electroencephalographic peculiarity: fronto-precentral beta wave groups [NCBI] 0.000134271
SGCG [NCBI] 0.000114959
LGMD2K [NCBI] 9.782e-05
creatine phosphokinase, elevated serum [NCBI] 9.04679e-05
LGMD1C [NCBI] 8.77575e-05
IBMPFD [NCBI] 8.54378e-05
scapuloperoneal syndrome, neurogenic, kaeser type [NCBI] 8.16093e-05
KCS [NCBI] 7.99895e-05
tibial muscular dystrophy, tardive [NCBI] 7.17329e-05
RMD [NCBI] 6.63054e-05
PDB [NCBI] 6.38696e-05
POMT1 [NCBI] 4.82238e-05
FKTN [NCBI] 4.82238e-05
TTN [NCBI] 4.38175e-05
MSTN [NCBI] 4.33226e-05
CAV3 [NCBI] 4.00649e-05
DES [NCBI] 3.78973e-05
VCP [NCBI] 3.68449e-05
LMNA [NCBI] 2.82978e-05
AGER [NCBI] 2.51707e-05
FTD [NCBI] 1.66248e-05




Database Center for Life Science