Reserved for future guideline expansion
D73.89
BookmarkOther diseases of spleen
Filed alongside this entry 15
under Ptosis
- breast N64.81
- brow H57.81
- cecum K63.4
- colon K63.4
- congenital (eyelid) Q10.0
- eyebrow H57.81
- gastric K31.89
- intestine K63.4
- kidney N28.83
- liver K76.89
- renal N28.83
- splanchnic K63.4
- spleen D73.89
- stomach K31.89
- viscera K63.4
Index entries, exactly as the book files them. This says they are listed together — not that any of them is documented in your chart.
Billable FY2027 2026-10-01 → 2027-09-30
How to use this page
Everything the published sources say about one code, on one page.
- Read the Excludes1 block first — it is the one that stops you coding this at all alongside another code.
- Excludes2, Code first, Use additional and Includes follow. A note inherited from a parent category is labelled with the category it came from, so you can see why it applies.
- Official Guidelines sit below. "Guidelines naming this code" cite the code or a range containing it; "Chapter guidance" is the general guidance for its chapter and is the weaker signal.
- Guideline text is quoted verbatim with its section number and page, so you can check it against the published document.
- Risk-model chips show which published CMS models map this code.
What this page does not do
- Guidance is quoted, never paraphrased — a paraphrase of a coding rule is a different rule.
- Medication candidates, where shown, are matched by condition *name* and are offered as candidates for you to judge. They are not "the drugs for this code".
Exclusions9never code together
D50-D89chapter
Excludes2
- autoimmune disease (systemic) NOS (M35.9)M35.9
- certain conditions originating in the perinatal period (P00-P96)P00-P96
- complications of pregnancy, childbirth and the puerperium (O00-O9A)O00-O9A
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)Q00-Q99
- endocrine, nutritional and metabolic diseases (E00-E88)E00-E88
- human immunodeficiency virus [HIV] disease (B20)B20
- injury, poisoning and certain other consequences of external causes (S00-T88)S00-T88
- neoplasms (C00-D49)C00-D49
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)R00-R94
Excludes2 — not included here, but the patient may have both. Code both when documented.
Instructional notes3
D73.89code
Inclusion terms
- Fibrosis of spleen NOS
- Perisplenitis
- Splenitis NOS
Official Guidelines1names this code
ICD-10-CM Official Guidelines for Coding and Reporting, quoted in full. Published by CMS and NCHS; in the public domain.
Index entries leading here21
- Deformity Q89.9
- spleen
- acquired D73.89
- spleen
- Calcification
- spleen D73.89
- Disease, diseased — see also Syndrome
- Episplenitis D73.89
- Fibrosis, fibrotic
- spleen D73.89
- Fistula (cutaneous) L98.8
- splenocolic D73.89
- Floating
- spleen D73.89
- Infection, infected, infective (opportunistic) B99.9
- spleen D73.89
- Inflammation, inflamed, inflammatory (with exudation)
- spleen (capsule) D73.89
- Lesion (s) (nontraumatic)
- spleen D73.89
- Lien migrans D73.89
- Movable
- spleen D73.89
- Perisplenitis (infectional) D73.89
- Prolapse, prolapsed
- spleen D73.89
- Ptosis — see also Blepharoptosis
- spleen D73.89
- Septic — see condition
- spleen (acute) D73.89
- Wandering
- spleen D73.89
- Splenitis (interstitial) (malignant) (nonspecific) D73.89
- Splenocele D73.89
- Splenoptosis D73.89
- Splenosis D73.89
Alongside this code1same parent — D73.8
Additional references
AHA Coding Clinic® Licence required
Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.