Hereditary spherocytosis
MONDO:0019350Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum (from symptom-free carriers to severe hemolysis) characterized by anemia, variable jaundice, splenomegaly and cholelithiasis.
Also known as: Minkowski-Chauffard disease, congenital spherocytic hemolytic anaemia, hereditary spherocytosis, spherocytic anaemia, congenital spherocytosis
11 clinical trials for this condition and its sub-types, 2 tagged with Hereditary spherocytosis itself.
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Sub-types of Hereditary spherocytosis
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Hereditary spherocytosis type 1 0 trials
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Hereditary spherocytosis type 2 0 trials
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Hereditary spherocytosis type 3 0 trials
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Hereditary spherocytosis type 4 0 trials
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Hereditary spherocytosis type 5 0 trials
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New study aims to personalize care for rare blood disorders
Knowledge-focused Recruiting nowThis study is for people with sickle cell disease or other rare anemias. Researchers want to use advanced genetic and blood tests to better understand each person's condition. The goal is to make diagnosis more precise so that treatments can be tailored to each patient. About 200…
Sponsor: Hospital Universitari Vall d'Hebron Research Institute • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:53 UTC
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Scientists probe Spleen's secrets to unlock blood disease mysteries
Knowledge-focused Recruiting nowThis study aims to better understand how the spleen filters and responds to abnormal blood cells in various diseases. Researchers will collect spleen tissue and blood from 100 adults undergoing planned splenectomy. By perfusing the spleen in the lab, they hope to uncover its role…
Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Knowledge-focused
Last updated Jun 26, 2026 16:56 UTC