5.1.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 1

AOA

Aminoacid and organic acids related disorders

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