Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Orotic Acid [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science