DB93.21 Idiopathic copper-associated cirrhosis
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2025-01
Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterised by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harbouring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining.
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
synonyms
- Idiopathic copper-associated cirrhosis
- Non-Wilsonian hepatic copper toxicosis of infancy and childhood
- Tyrolean infantile cirrhosis
- Idiopathic copper toxicosis
- Indian childhood cirrhosis
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