D76.3 is the ICD-10 code for Other histiocytosis syndromes. It is a four-character subcategory of D76 (Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue), the most specific level in the WHO edition. It belongs to the block D70–D77 (Other diseases of blood and blood-forming organs) 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 D76.3 includes
Conditions and terms that are coded here.
- Reticulohistiocytoma (giant-cell)
- Sinus histiocytosis with massive lymphadenopathy
- Xanthogranuloma
D76.3 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
- D76.3ARetikulohistiocytom (jättecells)
- D76.3BSinushistiocytos med massiv lymfadenopati [Rosai-Dorfman]
- D76.3CJuvenilt xantogranulom
- D76.3DNekrobiotiskt xantogranulom
- D76.3EBenign cefalisk histiocytos
- D76.3WAndra histiocytossyndrom
D76.3Annet histiocytosesyndrom
DD763Andet histiocytært syndrom
- DD763ARetikulohistiocytom (gigantocellulært)
- DD763BXanthogranulom
- DD763DSinus histiocytose med massiv lymfadenopati
D76.3Muu histiosytoosioireyhtymä
D76.3Sonstige Histiozytose-Syndrome
D76.3Autres syndromes histiocytaires
D76.3overige histiocytosesyndromen
D76.3Other histiocytosis syndromes
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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