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MeSH keywords -> Related genes, diseases (OMIM)


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01 Citrullinemia [NCBI]

Gene


 Gene Link Information
Gain		 01
SLC25A13 [NCBI] 0.000549255
ASS1 [NCBI] 8.4636e-05
SLC25A12 [NCBI] 2.59099e-05
SLC25A18 [NCBI] 1.46465e-05
SLC25A22 [NCBI] 1.37481e-05
ASL [NCBI] 1.09741e-05
SLC25A15 [NCBI] 1.03965e-05
SLC7A7 [NCBI] 9.89069e-06
SPINK1 [NCBI] 6.85416e-06



OMIM


 OMIM Link Information
gain		 01
citrullinemia, type ii, neonatal-onset [NCBI] 0.00110727
CTLN2 [NCBI] 0.00105368
ASS [NCBI] 0.0010083
SLC25A13 [NCBI] 0.000661886
citrullinemia, classic [NCBI] 0.000377157
argininosuccinic aciduria [NCBI] 7.87053e-05
hyperornithinemia-hyperammonemia-homocitrullinuria syndrome [NCBI] 7.51966e-05
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 5.80286e-05
ASL [NCBI] 5.21719e-05
SPINK1 [NCBI] 2.73252e-05



Database Center for Life Science