FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary spherocytosis ID (Ontology) DOID:12971 (Human Disease)
Definition A congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape.
Also Known As "Congenital spherocytic hemolytic anemia" ; "Minkowski Chauffard syndrome" ; "spherocytic anemia"
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physical disorder__
hemolytic anemia___|
                   congenital hemolytic anemia
                    |__hereditary spherocytosis  5 rec.
                        |__hereditary spherocytosis type 1 1 rec.
                        |__hereditary spherocytosis type 2 1 rec.
                        |__hereditary spherocytosis type 3 1 rec.
                        |__hereditary spherocytosis type 4 1 rec.
                        |__hereditary spherocytosis type 5 1 rec.
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Is a congenital hemolytic anemia
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Synonyms
  • "Congenital spherocytic hemolytic anemia" EXACT
    "Minkowski Chauffard syndrome" EXACT
    "spherocytic anemia" EXACT
Secondary IDs
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GARD:6639
ICD10CM:D58.0
ICD9CM:282.0
MESH:D013103
NCI:C97074
ORDO:822
SNOMEDCT_US_2023_03_01:154795009
UMLS_CUI:C0037889