3B80ICD-11 MMS 2026-01
Congenital disorders of spleen
Description
Any condition caused by a failure of the spleen to correctly develop in the antenatal period.
Index terms
- Congenital disorders of spleen
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
Child codes
3B80.0– Splenomegaly in storage diseases
Foundation children elsewhere
LB22– Structural developmental anomalies of spleen
Sibling codes
Foundation entity
Congenital disorders of spleen – http://id.who.int/icd/entity/1189893025
Part of: 03: Diseases of the blood or blood-forming organs