Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Kernicterus [NCBI]

Gene


 Gene Link Information
Gain		 01
G6PD [NCBI] 5.3492e-05
UGT1A1 [NCBI] 5.13025e-05
UGT1A9 [NCBI] 1.09873e-05
S100B [NCBI] 1.00725e-05
MAPT [NCBI] 6.23697e-06
GFAP [NCBI] 3.96868e-06
CASP3 [NCBI] 3.39133e-06
TNF [NCBI] 1.85391e-06



OMIM


 OMIM Link Information
gain		 01
fatty metamorphosis of viscera [NCBI] 0.00111789
crigler-najjar syndrome [NCBI] 0.000323251
G6PD [NCBI] 0.000286091
hyperbilirubinemia, transient familial neonatal [NCBI] 0.000105561
crigler-najjar syndrome, type ii [NCBI] 9.86293e-05
carbamoyl phosphate synthetase i deficiency, hyperammonemia due to [NCBI] 9.18269e-05
HSAN2 [NCBI] 9.18269e-05
robinow syndrome, autosomal recessive [NCBI] 8.84935e-05
UGT1A1 [NCBI] 4.76952e-05
ABCC1 [NCBI] 3.03295e-05
GFAP [NCBI] 1.08059e-05
TNF [NCBI] 2.37274e-06



Database Center for Life Science