ICD-10-CM Wilson's References

"Wilson's" Annotation Back-References in the ICD-10-CM Index to Diseases and Injuries

Browse the ICD-10-CM codes with references applicable to the clinical term "wilson's"

  • Wilson's
    • disease or syndrome - E83.01 Wilson's disease
    • hepatolenticular degeneration - E83.01 Wilson's disease
    • lichen ruber - L43.9 Lichen planus, unspecified

Applicable Clinical Terms Definitions

Hepatolenticular Degeneration: A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years.