Familial hemolytic anemia

Part of

Sub-types of Familial hemolytic anemia

• Congenital nonspherocytic hemolytic anemia 1 trial · 12 incl. sub-types
  10 sub-types

  • Pyruvate kinase deficiency of red cells 10 trials
  • Anemia, nonspherocytic hemolytic 0 trials · 2 incl. sub-types Sub-types →
  • Hemolytic anemia due to adenylate kinase deficiency 1 trial
  • Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency 1 trial
  • Gamma-glutamylcysteine synthetase deficiency 0 trials
  • Glutathione synthetase deficiency without 5-oxoprolinuria 0 trials
  • Hemolytic anemia due to erythrocyte adenosine deaminase overproduction 0 trials
  • Hemolytic anemia due to glucophosphate isomerase deficiency 0 trials
  • Hemolytic anemia due to glutathione reductase deficiency 0 trials
  • Non-spherocytic hemolytic anemia due to hexokinase deficiency 0 trials
• Congenital dyserythropoietic anemia 4 trials · 5 incl. sub-types
  9 sub-types

  • Congenital dyserythropoietic anemia type 1 1 trial Sub-types →
  • Congenital dyserythropoietic anemia type 2 1 trial
  • Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive 0 trials
  • X-linked dyserythropoetic anemia with abnormal platelets and neutropenia 0 trials
  • Anemia, congenital dyserythropoietic, type IVb 0 trials
  • Congenital dyserythropoietic anemia type 3 0 trials
  • Congenital dyserythropoietic anemia type 4 0 trials
  • Pancreatic insufficiency-anemia-hyperostosis syndrome 0 trials
  • Thrombocytopenia with congenital dyserythropoietic anemia 0 trials
• Abetalipoproteinemia 2 trials
• Cutaneous porphyria 2 trials
• Hereditary spherocytosis 2 trials
  5 sub-types

  • Hereditary spherocytosis type 1 0 trials
  • Hereditary spherocytosis type 2 0 trials
  • Hereditary spherocytosis type 3 0 trials
  • Hereditary spherocytosis type 4 0 trials
  • Hereditary spherocytosis type 5 0 trials
• Southeast Asian ovalocytosis 2 trials
• Glycogen storage disease VII 1 trial
• Glycogen storage disease due to aldolase A deficiency 1 trial
• Rh deficiency syndrome 0 trials
• X-linked congenital hemolytic anemia 0 trials
• Cryohydrocytosis 0 trials
• Dehydrated hereditary stomatocytosis 2 0 trials
• Dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema 0 trials
• Elliptocytosis 1 0 trials
• Elliptocytosis 2 0 trials
• Familial pseudohyperkalemia 0 trials
• Hemolytic anemia due to diphosphoglycerate mutase deficiency 0 trials
• Hemolytic disease of fetus and newborn, RH-induced 0 trials
• Hereditary cryohydrocytosis with reduced stomatin 0 trials
• Overhydrated hereditary stomatocytosis 0 trials
• Primary CD59 deficiency 0 trials
• Renal tubular acidosis, distal, 4, with hemolytic anemia 0 trials
• Triosephosphate isomerase deficiency 0 trials