hereditary spherocytosis

[autosomal dominant trait marked by splenomegaly, jaundice, and fragile, spheroid erythrocytes which are prematurely cleared by the spleen; anemia is usually mild; treatment is splenectomy. ( CSP )]

UMLS (CSP) C0037889

Disease or Syndrome

Relation/PAR: ANEMIA HEMOLITIKOA
Genetic Condition

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