Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hydroxocobalamin [NCBI]

Gene


 Gene Link Information
Gain		 01
MMACHC [NCBI] 5.52706e-06
CBLC [NCBI] 5.19861e-06
MTRR [NCBI] 4.07204e-06
ACADVL [NCBI] 2.35441e-06
CFH [NCBI] 1.77083e-06
HSPB1 [NCBI] 1.58104e-06
HMOX1 [NCBI] 1.45e-06
GJB2 [NCBI] 1.43513e-06
SLC6A4 [NCBI] 1.26776e-06
VWF [NCBI] 1.07824e-06



OMIM


 OMIM Link Information
gain		 01
methylmalonic aciduria and homocystinuria, cbld type [NCBI] 0.00501703
methylmalonic aciduria and homocystinuria, cblc type [NCBI] 0.00128274
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type [NCBI] 0.000480125
transcobalamin ii deficiency [NCBI] 0.000121179
megaloblastic anemia 1 [NCBI] 9.79079e-05
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency [NCBI] 9.38489e-05
MTRR [NCBI] 4.21038e-05
MTR [NCBI] 2.96216e-05



Database Center for Life Science