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MeSH keywords -> Related genes, diseases (OMIM)


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01 Chromium Isotopes [NCBI]


Gene


Gene Link Information
Gain
01
G6PD [NCBI] 3.37942e-06
HBD [NCBI] 2.12769e-06
GZMA [NCBI] 1.88583e-06
HBA1 [NCBI] 1.84223e-06
WAS [NCBI] 1.73739e-06
GZMB [NCBI] 1.60092e-06
CST3 [NCBI] 1.49586e-06




OMIM


OMIM Link Information
gain
01
stomatocytosis ii [NCBI] 0.00202368
splenic hypoplasia [NCBI] 0.00202368
CDAN3 [NCBI] 0.00160371
stomatocytosis i [NCBI] 0.0011173
CDAN2 [NCBI] 0.0011173
THC2 [NCBI] 0.000426283
HBB [NCBI] 0.00015519
glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to [NCBI] 0.000120837
complement factor i deficiency [NCBI] 0.000117986
WAS [NCBI] 0.00011421
crigler-najjar syndrome, type ii [NCBI] 0.000111108
erythrocytosis, familial, 2 [NCBI] 0.000109212
OPTB3 [NCBI] 0.000101568
OPTB1 [NCBI] 0.000101568
gilbert syndrome [NCBI] 9.91127e-05
glycogen storage disease vii [NCBI] 8.43063e-05
pyruvate kinase deficiency of red cells [NCBI] 7.85038e-05
LNS [NCBI] 7.58782e-05
G6PD [NCBI] 7.58294e-05
thrombocytopenic purpura, autoimmune [NCBI] 6.24339e-05
diphosphoglycerate mutase deficiency of erythrocyte [NCBI] 3.05451e-05
THY1 [NCBI] 2.88596e-05
CA2 [NCBI] 2.78131e-05
GZMA [NCBI] 2.69387e-05
GZMB [NCBI] 2.67408e-05
AK1 [NCBI] 2.52289e-05
anemia, sideroblastic, x-linked [NCBI] 2.50846e-05
HS [NCBI] 2.33924e-05
HBD [NCBI] 2.15709e-05
HPRT1 [NCBI] 1.86158e-05
HBA2 [NCBI] 1.78034e-05
HBA1 [NCBI] 1.30624e-05
TNFSF6 [NCBI] 6.23481e-06




Database Center for Life Science