Familial hemolytic anemia
MONDO:0003689A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.
Also known as: congenital hemolytic anemia, hereditary hemolytic anemia, anaemia hemolytic congenital, anemia hemolytic congenital
36 clinical trials for this condition and its sub-types, 4 tagged with Familial hemolytic anemia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Familial hemolytic anemia
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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
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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
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Abetalipoproteinemia 2 trials
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Cutaneous porphyria 2 trials
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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
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Southeast Asian ovalocytosis 2 trials
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Glycogen storage disease VII 1 trial
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Rh deficiency syndrome 0 trials
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X-linked congenital hemolytic anemia 0 trials
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Cryohydrocytosis 0 trials
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Elliptocytosis 1 0 trials
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Elliptocytosis 2 0 trials
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Familial pseudohyperkalemia 0 trials
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Primary CD59 deficiency 0 trials
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Triosephosphate isomerase deficiency 0 trials
Most studied deeper sub-types
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Could vitamin c tame anemia? early trial tests high doses in rare blood disorders
Disease control Not yet recruitingThis early-stage study tests whether high-dose Vitamin C is safe for people with two rare inherited blood disorders—Pyruvate Kinase Deficiency (PKD) and a form of G6PD deficiency. Both conditions cause red blood cells to break down too quickly, leading to anemia. The study will e…
Phase 1 • Sponsor: University of Utah • Aim: Disease control
Last updated Jun 27, 2026 12:39 UTC
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Robot-Assisted surgery showdown: which fix works best for rare bowel disease?
Disease control Not yet recruitingThis study compares two surgical techniques—Duhamel and Soave—for treating total colonic Hirschsprung disease, a severe birth defect where nerve cells are missing from the colon. Fifty children who had a first surgery as newborns will receive one of the two procedures. Researcher…
Sponsor: Zunyi Medical College • Aim: Disease control
Last updated Jun 27, 2026 08:11 UTC
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New hope for rare anemias: drug may cut transfusions
Disease control Not yet recruitingThis Phase 2 trial tests the drug luspatercept (Reblozyl) in 45 people with rare inherited anemias that affect red blood cells. The goal is to see if it can reduce the need for blood transfusions in those who depend on them, or raise hemoglobin levels in those who don't. Particip…
Phase 2 • Sponsor: EuroBloodNet Association • Aim: Disease control
Last updated Jun 27, 2026 08:10 UTC
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Smartwatch signals may flag anemia, no needle needed
Diagnosis Not yet recruitingAnemia often goes unnoticed because diagnosis requires a blood draw. This study tests whether a wrist-worn smartwatch can identify people likely to have anemia by tracking blood flow, heart rate, oxygen, and movement. About 400 adults, with and without anemia, will wear the watch…
Sponsor: Peking Union Medical College Hospital • Aim: Diagnosis
Last updated Sep 03, 2026 00:00 UTC
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Could a painless light sensor replace the needle for anemia screening?
Diagnosis Not yet recruitingThis study tests whether a non-invasive device that uses light to measure hemoglobin through the skin can accurately detect anemia. Researchers will compare its readings with standard blood tests in 150 adults in Jakarta. If the device proves reliable, it could offer a quick, pai…
Sponsor: Tarumanagara University • Aim: Diagnosis
Last updated Jul 17, 2026 00:00 UTC