Hereditary anemia

Part of

Sub-types of Hereditary anemia

• Vitamin B12- and folate-independent constitutional megaloblastic anemia 0 trials · 7 incl. sub-types
  2 sub-types

  • Thiamine-responsive megaloblastic anemia syndrome 6 trials
  • Orotic aciduria 1 trial Sub-types →
• Methylmalonic aciduria and homocystinuria 1 trial · 3 incl. sub-types
  6 sub-types

  • Methylmalonic aciduria and homocystinuria type cblC 3 trials
  • Methylmalonic aciduria and homocystinuria type cblD 2 trials
  • Methylmalonic acidemia with homocystinuria, type cblJ 1 trial
  • Methylmalonic aciduria and homocystinuria type cblF 1 trial
  • Methylmalonic acidemia with homocystinuria, type cblX 0 trials
  • Methylmalonic aciduria and homocystinuria, cb1L type 0 trials
• Homocystinuria without methylmalonic aciduria 0 trials · 2 incl. sub-types
  4 sub-types

  • Methylcobalamin deficiency type cblE 2 trials
  • Methylcobalamin deficiency type cblG 2 trials
  • Homocystinuria-megaloblastic anemia cblD type 0 trials
  • Methylcobalamin deficiency type cblDv1 0 trials
• Atransferrinemia 1 trial
• Hereditary intrinsic factor deficiency 1 trial
  1 sub-type

  • Intrinsic factor and r binder, combined congenital deficiency of 0 trials
• Transcobalamin II deficiency 1 trial
• IRIDA syndrome 0 trials
• Imerslund-Grasbeck syndrome 0 trials
  2 sub-types

  • Imerslund-Grasbeck syndrome type 1 0 trials
  • Imerslund-Grasbeck syndrome type 2 0 trials
• Aceruloplasminemia 0 trials
• Constitutional megaloblastic anemia with severe neurologic disease 0 trials
• Formiminoglutamic aciduria 0 trials
• Hereditary folate malabsorption 0 trials
• Microcytic anemia with liver iron overload 0 trials
• Severe congenital hypochromic anemia with ringed sideroblasts 0 trials