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MeSH keywords -> Related genes, diseases (OMIM)


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01 Reye Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
ECHS1 [NCBI] 1.66869e-05
NOS2 [NCBI] 1.38295e-05
HSD17B10 [NCBI] 1.22713e-05
FABP1 [NCBI] 1.09915e-05
IRF3 [NCBI] 1.03167e-05
FABP7 [NCBI] 8.8021e-06
MBP [NCBI] 5.58744e-06
TNF [NCBI] 2.86716e-06



OMIM


 OMIM Link Information
gain		 01
adrenal unresponsiveness to acth [NCBI] 0.00107364
fatty metamorphosis of viscera [NCBI] 0.000900049
acyl-coa dehydrogenase, medium-chain, deficiency of [NCBI] 0.000748343
ACADM [NCBI] 0.000354077
CDSP [NCBI] 0.000250695
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 0.000133825
ECHS1 [NCBI] 9.30442e-05
n-acetylglutamate synthase deficiency [NCBI] 9.09269e-05
3-@methylcrotonyl-coa carboxylase 1 deficiency [NCBI] 8.03344e-05
carbamoyl phosphate synthetase i deficiency, hyperammonemia due to [NCBI] 7.48942e-05
MTTH [NCBI] 6.6175e-05
MADD [NCBI] 6.54103e-05
glycogen storage disease v [NCBI] 6.34853e-05
IRF3 [NCBI] 5.52508e-05
SLC22A5 [NCBI] 5.41148e-05
3-@hydroxy-3-methylglutaryl-coa lyase deficiency [NCBI] 5.30958e-05
LPI [NCBI] 5.11736e-05
panencephalitis, subacute sclerosing [NCBI] 1.89634e-05
MBP [NCBI] 1.11911e-05
TNF [NCBI] 1.08189e-06



Database Center for Life Science