D58.0

Applicable To

• Acholuric familial) jaundice

• Congenital spherocytic) hemolytic icterus

• Minkowski-Chauffard syndrome

Approximate Synonyms

• Spherocytosis, hereditary

Clinical Information

• A familial congenital hemolytic anemia characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions.

• An autosomal dominant inherited disorder characterized by the presence of smaller than normal, sphere-shaped erythrocytes. It results in hemolytic anemia and splenomegaly.

• 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.

Details

• D58.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• The 2023 edition of ICD-10-CM D58.0 became effective on October 1, 2022.

• This is the American ICD-10-CM version of D58.0 – other international versions of ICD-10 D58.0 may differ.