Cure My Disease

Don't miss your cure!

 Log in / Sign up

Hereditary spherocytosis

MONDO:0019350

Hereditary 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

42 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Hereditary spherocytosis type 1 (0) Hereditary spherocytosis type 2 (0) Hereditary spherocytosis type 3 (0) Hereditary spherocytosis type 4 (0) Hereditary spherocytosis type 5 (0)

Broader categories

Disease (618) Anemia (203) Hereditary disease (172) Hematologic disorder (160) Hemolytic anemia (17) Human disease (14) Familial hemolytic anemia (3) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)
Trials to join now! 21 Not yet recruiting 2 Not yet finished but already full! 5 Completed 13 Terminated 1
Sort by