Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Thiamine Deficiency [NCBI]

Gene


 Gene Link Information
Gain		 01
SLC19A2 [NCBI] 6.06693e-05
CHAT [NCBI] 3.30156e-05
SST [NCBI] 3.08762e-05
SLC19A3 [NCBI] 2.85283e-05
ACHE [NCBI] 1.15295e-05
APLP2 [NCBI] 1.04384e-05
GFAP [NCBI] 9.71979e-06
APLP1 [NCBI] 9.5621e-06
ADH1B [NCBI] 8.34276e-06
ALDH2 [NCBI] 6.93362e-06
TH [NCBI] 4.58916e-06
CD68 [NCBI] 4.39406e-06



OMIM


 OMIM Link Information
gain		 01
wernicke-korsakoff syndrome [NCBI] 0.00230716
LS [NCBI] 0.000161039
SST [NCBI] 0.000145042
CHAT [NCBI] 0.000140712
cerebrocortical degeneration of infancy [NCBI] 0.000134657
TRMA [NCBI] 9.36381e-05
pyruvate decarboxylase deficiency [NCBI] 7.97993e-05
WFS1 [NCBI] 7.90724e-05
ACHE [NCBI] 4.10987e-05
GFAP [NCBI] 3.13012e-05
TH [NCBI] 1.37758e-05
VEGF [NCBI] 9.48402e-07



Database Center for Life Science