Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hyperammonemia	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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