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MeSH keywords -> Related genes, diseases (OMIM)


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01 Wernicke Encephalopathy [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 5.28348e-05
TKT [NCBI] 1.49174e-05
GFAP [NCBI] 1.389e-05
APLP2 [NCBI] 1.24271e-05
APLP1 [NCBI] 1.15501e-05
MAPT [NCBI] 7.89316e-06
APOE [NCBI] 5.17188e-06



OMIM


 OMIM Link Information
gain		 01
wernicke-korsakoff syndrome [NCBI] 0.00603512
alaninuria with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus [NCBI] 0.000133535
leigh syndrome, x-linked [NCBI] 0.000128028
lactic acidosis, fatal infantile [NCBI] 0.000115632
TKTL1 [NCBI] 9.19492e-05
CHAC [NCBI] 8.99842e-05
TKT [NCBI] 7.71931e-05
LS [NCBI] 7.49402e-05
GFAP [NCBI] 5.62884e-05
CJD [NCBI] 3.52955e-05
APOE [NCBI] 2.08784e-05



Database Center for Life Science