D73.1

Hypersplenism

Coding guidance (WHO 2019)

Excl.: splenomegaly: NOS (R16.1) congenital (Q89.0)

Sibling codes

D73Diseases of spleen D73.0Hyposplenism D73.2Chronic congestive splenomegaly D73.3Abscess of spleen D73.4Cyst of spleen D73.5Infarction of spleen D73.8Other diseases of spleen D73.9Disease of spleen, unspecified