D73.89
Other diseases of spleen
This code does not map to a risk-adjusting HCC in the loaded models.
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
Fibrosis of spleen NOS Perisplenitis Splenitis NOS
autoimmune disease (systemic) NOS (M35.9) certain conditions originating in the perinatal period (P00-P96) complications of pregnancy, childbirth and the puerperium (O00-O9A) congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) endocrine, nutritional and metabolic diseases (E00-E88) human immunodeficiency virus [HIV] disease (B20) injury, poisoning and certain other consequences of external causes (S00-T88) neoplasms (C00-D49) symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Official Guidelines for D73.89
FY 2026 ›Find D73.89 in the alphabetic index
21 index paths lead to this code
- Episplenitis
- Lien migrans
- Perisplenitis
- Splenitis
- Splenocele
- Splenoptosis
- Splenosis
- Calcification › spleen
- Fibrosis, fibrotic › spleen
- Fistula › splenocolic
- Floating › spleen
- Infection, infected, infective › spleen
- Inflammation, inflamed, inflammatory › spleen
- Lesion › spleen
- Movable › spleen
- Prolapse, prolapsed › spleen
- Ptosis › spleen
- Septic › spleen
- Wandering › spleen
- Deformity › spleen › acquired
- Disease, diseased › spleen › postinfectional