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2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders 240-279 > Other Metabolic Disorders And Immunity Disorders 270-279 > Disorders Of Mineral Metabolism 275.* >

2007 ICD-9-CM Diagnosis 275.1

Disorders of copper metabolism

This code may be outdated. View the most recent version of ICD-9-CM 275.1

  • 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.
  • 275.1 is a specific code that can be used to specify a diagnosis
  • 275.1 contains 24 index entries
  • View the ICD-9-CM Volume 1 275.* hierarchy

275.1 also known as:

  • Hepatolenticular degeneration
  • Wilson's disease

Index entries containing 275.1:

Cirrhosis, cirrhotic 571.5
  • due to
    • hepatolenticular degeneration 275.1
    • Wilson's disease 275.1
Deficiency, deficient
  • ceruloplasmin 275.1
  • copper NEC 275.1
Degeneration, degenerative
  • hepatolenticular (Wilson's) 275.1
  • lenticular (familial) (progressive) (Wilson's) (with cirrhosis of liver) 275.1
  • Wilson's hepatolenticular 275.1
Disease, diseased - see also Syndrome
  • hepatolenticular 275.1
  • Kinnier Wilson's (hepatolenticular degeneration) 275.1
  • Wilson's (hepatolenticular degeneration) 275.1
Disorder - see also Disease
  • metabolism NEC 277.9
    • copper 275.1
Hepatolenticular degeneration 275.1
Kinnier Wilson's disease (hepatolenticular degeneration) 275.1
Lenticular degeneration, progressive 275.1
Pseudosclerosis (brain)
  • of Westphal (-Strümpell) (hepatolenticular degeneration) 275.1
Strümpell-Westphal pseudosclerosis (hepatolenticular degeneration) 275.1
Syndrome - see also Disease
  • amyostatic 275.1
  • chorea-athetosis-agitans 275.1
  • lenticular 275.1
  • Westphal-Strümpell (hepatolenticular degeneration) 275.1
  • Wilson's (hepatolenticular degeneration) 275.1
Westphal-Strümpell syndrome (hepatolenticular degeneration) 275.1
Wilson's
  • disease or syndrome (hepatolenticular degeneration) 275.1
  • hepatolenticular degeneration 275.1