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MeSH keywords -> Related genes, diseases (OMIM)


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01 Wolff-Parkinson-White Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
TRNL1 [NCBI] 0.000287562
PRKAG2 [NCBI] 0.000124897
ND5 [NCBI] 2.62806e-05
PRKAB1 [NCBI] 1.16239e-05
PRKAA1 [NCBI] 1.14891e-05
PRKAA2 [NCBI] 1.09873e-05
LAMP2 [NCBI] 1.04168e-05
FABP3 [NCBI] 9.76214e-06
MYH7 [NCBI] 8.99365e-06
KCNQ1 [NCBI] 7.34997e-06
CRP [NCBI] 6.97873e-06
IL8 [NCBI] 6.39006e-06
IL6 [NCBI] 4.84255e-06



OMIM


 OMIM Link Information
gain		 01
wolff-parkinson-white syndrome [NCBI] 0.00156399
ASD1 [NCBI] 0.00114043
PRKAG2 [NCBI] 0.00066644
cardiomyopathy, familial hypertrophic, with wolff-parkinson-white syndrome [NCBI] 0.000474197
LS [NCBI] 0.000117785
leber optic atrophy [NCBI] 9.54414e-05
CMD1A [NCBI] 5.93712e-05
MTND5 [NCBI] 5.69272e-05
glycogen storage disease ii [NCBI] 4.74833e-05
MTTL1 [NCBI] 4.33619e-05
TS [NCBI] 2.05182e-05



Database Center for Life Science