Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hyperbilirubinemia, Hereditary [NCBI]

Gene


 Gene Link Information
Gain		 01
UGT1A1 [NCBI] 0.000173511
ABCC2 [NCBI] 1.80712e-05
G6PD [NCBI] 1.28423e-05
SLCO1B1 [NCBI] 1.1301e-05
UGT1A9 [NCBI] 1.06645e-05
PPOX [NCBI] 9.13686e-06
ENG [NCBI] 6.28586e-06
GFAP [NCBI] 3.65911e-06



OMIM


 OMIM Link Information
gain		 01
hyperbilirubinemia, rotor type [NCBI] 0.00510184
gilbert syndrome [NCBI] 0.00134694
crigler-najjar syndrome [NCBI] 0.000797009
crigler-najjar syndrome, type ii [NCBI] 0.000649724
DJS [NCBI] 0.000392495
UGT1A1 [NCBI] 0.000340673
hyperbilirubinemia, transient familial neonatal [NCBI] 0.000186324
ABCC2 [NCBI] 0.000112812
fructose-1,6-bisphosphatase deficiency [NCBI] 7.36018e-05
galactokinase deficiency [NCBI] 6.77742e-05
ALGS1 [NCBI] 4.47514e-05
HBB [NCBI] 2.35286e-05
G6PD [NCBI] 1.88267e-05
GFAP [NCBI] 1.17628e-05



Database Center for Life Science