3B81.BICD-11 MMS 2026-01
Hypersplenism
Description
A disease caused by determinants such as cirrhosis, malaria, tuberculosis or inflammatory disorders leading overactive spleen function. This disease is characterised by the presence of an enlarged spleen. Confirmation is by identification through medical imaging.
Index terms
- Hypersplenism
- big spleen syndrome
- hyperfunction of spleen
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- hypersplenia
- increased splenic activity
- spleen metaplasia
- splenic metaplasia
- Gamna disease
- Gandy Nanta disease
- Splenic primary panhaematopenia
- Myeloid metaplasia
- Agnogenic myeloid metaplasia
- Myelogenous metaplasia
Excludes
Exclusions from above levels
04– Diseases of the immune system05– Endocrine, nutritional or metabolic diseases18– Complications of pregnancy, childbirth or the puerperium
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19– Certain conditions originating in the perinatal period20– Congenital malformations, deformations or chromosomal abnormalities22– Injury, poisoning or certain other consequences of external causes- http://id.who.int/icd/entity/1000704511 – Human immunodeficiency virus disease
JB64.1– Other diseases of the blood or blood-forming organs or certain disorders involving the immune mechanism complicating pregnancy, childbirth or the puerperium
Sibling codes
3B81.0– Tumour-like conditions of spleen3B81.1– Postsurgical asplenia3B81.2– Atrophy of spleen3B81.3– Nontraumatic laceration or rupture of spleen3B81.4– Splenosis3B81.5– Splenic cyst or pseudocyst3B81.6– Infarction of spleen3B81.7– Infection of spleen3B81.8– Torsion of spleen3B81.9– Fibrosis of spleen3B81.A– Perisplenitis3B81.C– Chronic congestive splenomegaly3B81.Y– Other specified acquired disorders of spleen3B81.Z– Acquired disorders of spleen, unspecified
Foundation entity
Part of: 3B81: Acquired disorders of spleen › 03: Diseases of the blood or blood-forming organs