D58.0 is the ICD-10 code for Hereditary spherocytosis. It is a four-character subcategory of D58 (Other hereditary haemolytic anaemias), the most specific level in the WHO edition. It belongs to the block D55–D59 (Haemolytic anaemias) in Chapter III, Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism.
- Code type
- Subcategory (4 characters)
- Chapter
- III · D50–D89
- Classification
- WHO ICD-10, 2019 version
What D58.0 includes
Conditions and terms that are coded here.
- Acholuric (familial) jaundice
- Congenital (spherocytic) haemolytic icterus
- Minkowski-Chauffard syndrome
D58.0 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
D58.0Hereditär sfärocytos
D58.0Arvelig sfærocytose
DD580Arvelig hæmolytisk anæmi forårsaget af sfærocytose
D58.0Perinnöllinen pallosoluisuus
D58.0Hereditäre Sphärozytose
D58.0Sphérocytose héréditaire
D58.0hereditaire sferocytose
D58.0Hereditary spherocytosis
Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.
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