MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
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