PH3039 Hereditary spherocytosis diagnosis codes
OpenCodelists Phenotype
Last updated 2026-01-26 NHSD Primary Care Domain Refsets
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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.
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