Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Paralyses, Familial Periodic [NCBI]

Gene


 Gene Link Information
Gain		 01
SCN4A [NCBI] 0.000298155
KCNJ2 [NCBI] 7.15329e-05
KCNE3 [NCBI] 6.30054e-05
CACNA1S [NCBI] 6.04045e-05
KCNC4 [NCBI] 4.29991e-05
KCNJ12 [NCBI] 2.69048e-05
KCNJ4 [NCBI] 1.31647e-05
MPZL1 [NCBI] 1.31647e-05
KCNJ3 [NCBI] 1.20977e-05
KCNJ6 [NCBI] 1.04975e-05
KCNA1 [NCBI] 8.95737e-06
CLCN1 [NCBI] 7.67801e-06
MB [NCBI] 6.94263e-06
DMPK [NCBI] 5.37166e-06



OMIM


 OMIM Link Information
gain		 01
HYPP [NCBI] 0.00267132
HOKPP [NCBI] 0.00137456
EMWX [NCBI] 0.00129156
malignant hyperthermia, susceptibility to, 2 [NCBI] 0.000898321
andersen cardiodysrhythmic periodic paralysis [NCBI] 0.000889558
myopathy, tubular aggregate [NCBI] 0.000817902
SCN4A [NCBI] 0.0006719
PMC [NCBI] 0.000602573
thyrotoxic periodic paralysis [NCBI] 0.00055699
CACNA1S [NCBI] 0.000345844
KCNE3 [NCBI] 0.000229527
KCNJ2 [NCBI] 0.000190681
myotonia, potassium-aggravated [NCBI] 0.000159
PRPS2 [NCBI] 8.71994e-05
opitz syndrome [NCBI] 6.5372e-05
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 1 [NCBI] 5.85685e-05
MCOPS7 [NCBI] 4.56826e-05
OA1 [NCBI] 4.10261e-05
CMT1B [NCBI] 3.69846e-05
MB [NCBI] 2.97266e-05



Database Center for Life Science