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01 Oculomotor Muscles [NCBI]


Gene


Gene Link Information
Gain
01
OPEM [NCBI] 0.000442596
FEOM3 [NCBI] 0.000442596
TUKLS [NCBI] 0.000442596
KTWS [NCBI] 0.000273994
KIF21A [NCBI] 0.000133595
PHOX2A [NCBI] 4.99599e-05
MYH13 [NCBI] 2.52899e-05
APTX [NCBI] 1.90303e-05
MS [NCBI] 1.87849e-05
MYOM2 [NCBI] 1.55688e-05
LMOD1 [NCBI] 1.54303e-05
ACHE [NCBI] 1.48523e-05
CHN1 [NCBI] 1.37262e-05
ATP2A1 [NCBI] 1.10989e-05
PAX7 [NCBI] 1.09867e-05
MYOG [NCBI] 8.93005e-06
DMPK [NCBI] 7.88701e-06
MYOD1 [NCBI] 7.53111e-06
CHAT [NCBI] 6.78126e-06
MYOM1 [NCBI] 6.35948e-06
SALL4 [NCBI] 5.88361e-06
TG [NCBI] 5.79231e-06
MYH6 [NCBI] 5.6443e-06
CA3 [NCBI] 5.60262e-06
ACTN3 [NCBI] 5.45139e-06
PABPN1 [NCBI] 5.41691e-06
TMOD1 [NCBI] 5.38358e-06
SSPN [NCBI] 5.35133e-06
COCH [NCBI] 5.0758e-06
ACAN [NCBI] 4.9201e-06
THRB [NCBI] 4.6355e-06
CAV3 [NCBI] 4.59015e-06
THRA [NCBI] 4.53272e-06
TIMP2 [NCBI] 4.3314e-06
RHO [NCBI] 4.27603e-06
RYR1 [NCBI] 4.2236e-06
TSHR [NCBI] 4.19342e-06
ATP2A2 [NCBI] 4.1738e-06
CACNA1A [NCBI] 3.87439e-06
TIMP1 [NCBI] 3.83915e-06
MUSK [NCBI] 3.74672e-06
SNAP25 [NCBI] 3.61702e-06
ATXN1 [NCBI] 3.60059e-06
SST [NCBI] 3.46393e-06
PAX3 [NCBI] 3.46393e-06
DAG1 [NCBI] 3.14112e-06
ICAM1 [NCBI] 3.08512e-06
FOXO1 [NCBI] 3.02313e-06
MMP2 [NCBI] 2.80634e-06
SLC5A5 [NCBI] 2.78736e-06
NEFH [NCBI] 2.63971e-06
BMP7 [NCBI] 2.61785e-06
BMP4 [NCBI] 2.49804e-06
NPY [NCBI] 2.48091e-06
TRH [NCBI] 1.33592e-06
HGF [NCBI] 1.1574e-06
BDNF [NCBI] 9.90161e-07
VIP [NCBI] 9.20556e-07




OMIM


OMIM Link Information
gain
01
CFEOM3 [NCBI] 0.00860956
OPMD [NCBI] 0.00602572
CFEOM1 [NCBI] 0.00186219
duane retraction syndrome 2 [NCBI] 0.00173626
strabismus, susceptibility to [NCBI] 0.00173626
MG [NCBI] 0.00137932
tukel syndrome [NCBI] 0.00128958
OPEM [NCBI] 0.00128958
CFEOM3B [NCBI] 0.00128958
CFEOM3A [NCBI] 0.00128958
wieacker syndrome [NCBI] 0.000862604
ocular motor apraxia [NCBI] 0.000787075
inclusion body myositis [NCBI] 0.00068662
NNO1 [NCBI] 0.00068662
fibrosis of extraocular muscles, congenital, with synergistic divergence [NCBI] 0.000515349
CFEOM2 [NCBI] 0.000515349
RA [NCBI] 0.000398248
MBS [NCBI] 0.000382199
SPS [NCBI] 0.000382199
EAOH [NCBI] 0.000303466
KSS [NCBI] 0.000208618
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive [NCBI] 0.00019615
vestibulocochlear dysfunction, progressive [NCBI] 0.000171545
ophthalmoplegia, familial total, with iris transillumination [NCBI] 0.000171545
MYH13 [NCBI] 0.000163021
camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye [NCBI] 0.000132334
APTX [NCBI] 0.000128864
SLE [NCBI] 0.000112933
gaucher disease, type iiic [NCBI] 0.000108014
axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities [NCBI] 0.000108014
PABPN1 [NCBI] 9.22345e-05
SPMM [NCBI] 9.06051e-05
minicore myopathy with external ophthalmoplegia [NCBI] 8.31255e-05
MNGIE [NCBI] 7.03398e-05
EA2 [NCBI] 6.83807e-05
graves disease [NCBI] 6.65567e-05
DLB [NCBI] 6.32498e-05
ACHE [NCBI] 6.17702e-05
SCA6 [NCBI] 5.31118e-05
KIF21A [NCBI] 5.22273e-05
SJS1 [NCBI] 5.01591e-05
SCA2 [NCBI] 4.36795e-05
MTM1 [NCBI] 3.39734e-05
MTM1 [NCBI] 3.20029e-05
ICAM1 [NCBI] 3.09187e-05
FN1 [NCBI] 3.06715e-05
SCA1 [NCBI] 3.05559e-05
GBA [NCBI] 2.75708e-05
TG [NCBI] 2.61917e-05
CHAT [NCBI] 2.6055e-05
RYR1 [NCBI] 2.57772e-05
GDNF [NCBI] 2.23774e-05
RHO [NCBI] 2.22942e-05
DMD [NCBI] 1.97734e-05
NF1 [NCBI] 1.78553e-05
SST [NCBI] 1.75143e-05
SLC18A3 [NCBI] 1.72251e-05
DMD [NCBI] 1.3673e-05
dystrophia myotonica 1 [NCBI] 1.33783e-05
GAL [NCBI] 1.1659e-05
MJD [NCBI] 1.07526e-05
PD [NCBI] 8.82225e-06
NPY [NCBI] 5.00111e-06
TNFSF6 [NCBI] 4.95005e-06
HGF [NCBI] 2.27965e-06
BDNF [NCBI] 1.37696e-06
VIP [NCBI] 1.03749e-06
VEGF [NCBI] 5.29462e-07
RP [NCBI] 1.25127e-08




Database Center for Life Science