Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hyperammonemia [NCBI]

Gene


 Gene Link Information
Gain		 01
GLUDP5 [NCBI] 0.0011722
SLC25A15 [NCBI] 0.000187105
NAGS [NCBI] 9.37927e-05
GLUD1 [NCBI] 8.71435e-05
SLC25A2 [NCBI] 5.86718e-05
OTC [NCBI] 3.33528e-05
ALDH18A1 [NCBI] 2.92521e-05
OAT [NCBI] 1.92642e-05
GLUD2 [NCBI] 1.37072e-05
PYCR1 [NCBI] 1.15957e-05
SLC25A20 [NCBI] 1.14046e-05
CPS1 [NCBI] 1.12326e-05
ASL [NCBI] 1.09332e-05
MUT [NCBI] 9.92444e-06
TSPO [NCBI] 9.14241e-06
SLC25A13 [NCBI] 8.75516e-06
ACCN4 [NCBI] 7.67777e-06
GRM5 [NCBI] 6.16675e-06
CNTF [NCBI] 5.30116e-06
SLC2A1 [NCBI] 4.83747e-06
CAT [NCBI] 3.19366e-06
GFAP [NCBI] 2.24742e-06



OMIM


 OMIM Link Information
gain		 01
HHF6 [NCBI] 0.000495726
NAGS [NCBI] 0.000320278
hyperornithinemia-hyperammonemia-homocitrullinuria syndrome [NCBI] 0.000191281
GLUD1 [NCBI] 0.000125409
OTC [NCBI] 0.00011587
n-acetylglutamate synthase deficiency [NCBI] 0.000101727
PDV [NCBI] 9.39491e-05
PYCS [NCBI] 9.09049e-05
ALMS [NCBI] 7.89629e-05
SLC25A15 [NCBI] 6.60373e-05
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 6.59046e-05
CPS1 [NCBI] 6.09492e-05
SLC6A6 [NCBI] 5.76039e-05
ASL [NCBI] 5.58717e-05
3-@hydroxy-3-methylglutaryl-coa lyase deficiency [NCBI] 5.09606e-05
CNTF [NCBI] 2.35836e-05
CAT [NCBI] 1.21041e-05
GFAP [NCBI] 6.83558e-06



Database Center for Life Science