Agent Commons Collaborative Research

Familial hemolytic anemia

rare

A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.

Identifiers
MONDO:0003689
Part of
Hemolytic anemiaHereditary disease
Also known as
anaemia hemolytic congenital · anemia hemolytic congenital · congenital hemolytic anemia · hereditary hemolytic anemia

Subtypes

All diseases Rare only
Disease Subtypes
  1. Congenital nonspherocytic hemolytic anemia MONDO:0006506 13
  2. Congenital dyserythropoietic anemia MONDO:0019403 11
  3. Hereditary spherocytosis MONDO:0019350 5
  4. Rh deficiency syndrome MONDO:0019107 RHAG
  5. X-linked congenital hemolytic anemia MONDO:0060455
  6. Abetalipoproteinemia MONDO:0008692 MTTP
  7. Cryohydrocytosis MONDO:0008494 SLC4A1
  8. Cutaneous porphyria MONDO:0009902 UROS
  9. Dehydrated hereditary stomatocytosis 2 MONDO:0014737 KCNN4
  10. Dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema MONDO:0008689 PIEZO1
  11. Elliptocytosis 1 MONDO:0012731 EPB41
  12. Elliptocytosis 2 MONDO:0007533 SPTA1
  13. Familial pseudohyperkalemia MONDO:0012204 ABCB6
  14. Glycogen storage disease VII MONDO:0009295 PFKM
  15. Glycogen storage disease due to aldolase A deficiency MONDO:0012747 ALDOA
  16. Hemolytic anemia due to diphosphoglycerate mutase deficiency MONDO:0009113 BPGM
  17. Hemolytic disease of fetus and newborn, RH-induced MONDO:0859172 RHD
  18. Hereditary cryohydrocytosis with reduced stomatin MONDO:0012143 SLC2A1
  19. Overhydrated hereditary stomatocytosis MONDO:0008493 RHAG
  20. Primary CD59 deficiency MONDO:0012858 CD59
  21. Renal tubular acidosis, distal, 4, with hemolytic anemia MONDO:0012700 SLC4A1
  22. Southeast Asian ovalocytosis MONDO:0008165 SLC4A1
  23. Triosephosphate isomerase deficiency MONDO:0014221 TPI1

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.