5.01.i
Disorders of cobalamin metabolism
- Hereditary intrinsic factor deficiency
- Cubilin deficiency (Imerslund-Gräsbeck disease, Finnish type)
- Amnionless deficiency (Imerslund-Gräsbeck disease, Norwegian type)
- Haptocorrin deficiency (Transcobalamin I deficiency)
- Transcobalamin II deficiency
- Transcobalamin receptor deficiency
- Methylmalonic aciduria and homocystinuria, cblF type
- Methylmalonic aciduria and homocystinuria, cblJ type
- Methylmalonic aciduria and homocystinuria, cblC type
- Epi-cblC
- Methylmalonic aciduria and homocystinuria, cblD type
- Homocystinuria, cblDv1 type
- Methylmalonic aciduria, cblDv2 type
- Methylmalonic aciduria, cblA type
- Methylmalonic aciduria, cblB type
- Methionine synthase reductase deficiency (Homocystinuria-megaloblastic anemia, cblE type)
- Methylmalonic aciduria and homocystinuria, cblX type
- Methylmalonic aciduria and homocystinuria due to ZNF143 deficiency
- Methylmalonic aciduria and homocystinuria due to Ronin deficiency
Subnetworks
AOA
Aminoacid and organic acids related disorders
