Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Epilepsy, Benign Neonatal [NCBI]

Gene


 Gene Link Information
Gain		 01
BFIC [NCBI] 0.00327841
KCNQ2 [NCBI] 0.000423643
BFIC2 [NCBI] 0.000362052
KCNQ3 [NCBI] 0.000178816
SCN2A [NCBI] 7.86674e-05
KCNQ5 [NCBI] 2.64357e-05
KCNQ4 [NCBI] 2.06737e-05
ATP1A2 [NCBI] 1.76176e-05
SLC5A11 [NCBI] 1.44146e-05
GABRD [NCBI] 1.16199e-05
SCO1 [NCBI] 1.07424e-05
GABRR2 [NCBI] 1.06102e-05
WASF2 [NCBI] 9.97915e-06
SCO2 [NCBI] 9.519e-06
GABRG2 [NCBI] 9.45303e-06
SCN1B [NCBI] 9.32827e-06
SLC5A1 [NCBI] 8.64338e-06
EPM2A [NCBI] 8.18634e-06
SCN1A [NCBI] 7.65979e-06
PTGES2 [NCBI] 6.06381e-06



OMIM


 OMIM Link Information
gain		 01
convulsions, benign familial infantile, 2 [NCBI] 0.00236515
convulsions, benign familial infantile, 1 [NCBI] 0.00170705
EBN3 [NCBI] 0.00116675
ICCA [NCBI] 0.000813359
epilepsy, nocturnal frontal lobe, type 2 [NCBI] 0.000773718
KCNQ2 [NCBI] 0.000569008
EBN1 [NCBI] 0.00055536
seizures, benign familial neonatal-infantile [NCBI] 0.000385493
SCN2A [NCBI] 0.000234179
GEFS+ [NCBI] 0.000188175
myokymia with neonatal epilepsy [NCBI] 0.000122684
epilepsy, nocturnal frontal lobe, type 3 [NCBI] 0.000114204
pyridoxamine 5-prime-phosphate oxidase deficiency [NCBI] 0.000114204
EBN2 [NCBI] 0.000108698
epilepsy, nocturnal frontal lobe, type 1 [NCBI] 9.4278e-05
SLC5A11 [NCBI] 9.30442e-05
EPD [NCBI] 8.45465e-05
FHM2 [NCBI] 8.16836e-05
SMEI [NCBI] 6.90246e-05
GABRG2 [NCBI] 6.18421e-05
ATP1A2 [NCBI] 5.72439e-05
RTT [NCBI] 3.99074e-05



Database Center for Life Science