Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Orotic Acid	[NCBI]

Gene	Link	Information Gain
APOB	[NCBI]	4.25766e-06
NAGS	[NCBI]	4.24271e-06
OAT	[NCBI]	3.85745e-06
TAT	[NCBI]	3.29901e-06
EGF	[NCBI]	2.43993e-06
DHODH	[NCBI]	2.26963e-06
UMPS	[NCBI]	2.1699e-06
UPRT	[NCBI]	2.06341e-06
FZD1	[NCBI]	2.02619e-06
ASL	[NCBI]	1.84252e-06
OTC	[NCBI]	1.80966e-06
GCNT1	[NCBI]	1.75656e-06
PPT2	[NCBI]	1.74661e-06
RECQL	[NCBI]	1.73004e-06
MGAT3	[NCBI]	1.72548e-06
CAD	[NCBI]	1.62048e-06
AGXT2L1	[NCBI]	1.58891e-06
CYP2C8	[NCBI]	1.50386e-06
CHEK2	[NCBI]	1.24257e-06
CHEK1	[NCBI]	1.21826e-06
AHR	[NCBI]	1.13982e-06
CYP2C9	[NCBI]	1.13314e-06
TRH	[NCBI]	8.91965e-07

OMIM	Link	Information gain
ornithine transcarbamylase deficiency, hyperammonemia due to	[NCBI]	0.00136344
VRNI	[NCBI]	0.000798761
orotic aciduria i	[NCBI]	0.000720986
orotic aciduria ii	[NCBI]	0.000323857
LPI	[NCBI]	0.000260075
hyperornithinemia-hyperammonemia-homocitrullinuria syndrome	[NCBI]	0.000219328
n-acetylglutamate synthase deficiency	[NCBI]	0.000106822
argininemia	[NCBI]	8.67029e-05
citrullinemia, classic	[NCBI]	7.74075e-05
OTC	[NCBI]	5.09316e-05
APOB	[NCBI]	3.78854e-05
PRPS1	[NCBI]	2.95517e-05
LCAT	[NCBI]	2.90019e-05
NP	[NCBI]	2.11232e-05
ASL	[NCBI]	2.06573e-05
ASS	[NCBI]	1.8301e-05
AHR	[NCBI]	7.22503e-06
EGF	[NCBI]	4.98206e-06