Hereditary spherocytosis

Orpha code: 822OMIM code: 616649

Definition

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.

Disease data
Classification

Disease

Synonyms
Minkowski-Chauffard disease
Choroba Minkowskiego i Chauffarda
ORPHA code
822
OMIM code
616649
ICD10 code
D58.0
ICD11 code
3A10.Y

No additional description.

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