AutoICD API

E83.01

Billable

Wilson's disease

Wilson's disease

Status

Billable / Specific

Block

E70-E88

Parent Code

E83.0

Coding Notes

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Code Also

A second code may be required; sequencing depends on circumstances

Related Codes(2)
E83.00

Disorder of copper metabolism, unspecified

BillableE83.09

Other disorders of copper metabolism

Billable
Also Known As / Clinical Terms(193)

SNOMED CT

UMLS

Clinical Terms

  • Progressive lenticular degeneration
  • Westphal-Strumpell cerebral pseudosclerosis
  • Degeneration Syndromes, Hepatolenticular
  • Kinnier-Wilson disease
  • hepato-lenticular degeneration
  • Hepatolenticular Degeneration Syndromes
  • Westphal-Strumpell Syndrome
  • Hepatocerebral Degeneration
  • Dementia due to Wilson's disease
  • Chorea co-occurrent and due to Wilson disease
  • Dementia due to hepatolenticular degeneration
  • Hepato-Neurologic Wilson Diseases
  • WILSONS DIS
  • Hypoparathyroidism due to Wilson disease
  • Wilson Disease
  • Diseases, Copper Storage
  • Chorea due to metabolic disorder
  • Wilsons Disease
  • Degeneration, Neurohepatic
  • Disorder of liver due to disorder of mineral metabolism
  • diseases wilson
  • Hepatolenticular Degeneration Syndrome
  • disease wilson's
  • HEPATONEUROLOGIC WILSON DIS
  • Chorea with Wilson disease
  • Diseases, Kinnier-Wilson
  • Syndromes, Hepatolenticular Degeneration
  • WD - Wilson's disease
  • Westphal Strumpell disease
  • Copper storage disease
  • WND
  • Dementia due to metabolic abnormality
  • Westphal pseudosclerosis
  • Hepatolenticular degeneration
  • Wilson Disease, Hepato-Neurologic
  • Kinnier Wilson Disease
  • Degenerations, Neurohepatic
  • Pseudosclerosis
  • Gowers' chorea
  • Cerebral Pseudosclerosis
  • Wilson Diseases, Hepato-Neurologic
  • Copper Storage Diseases
  • Neurohepatic degeneration
  • Disorder of copper metabolism
  • Hepatocerebral Degenerations
  • Dementia due to Wilson disease
  • KINNIER WILSON DIS
  • Degenerations, Hepatocerebral
  • familial hepatitis
  • Disease, Copper Storage
  • WILSON DIS
  • Degeneration, Hepatocerebral
  • Pseudosclerosis, Cerebral
  • Degeneration Syndrome, Hepatolenticular
  • Chorea due to heredodegenerative disorder
  • Westphal Strumpell Syndrome
  • Neurohepatic Degenerations
  • Dystonia due to Wilson disease
  • Dementia due to genetic disease
  • disease wilsons
  • Westphal-Strumpell syndrome (disorder)
  • Copper metabolism disorder
  • Pseudoscleroses, Cerebral
  • Cerebral Pseudoscleroses
  • Syndrome, Hepatolenticular Degeneration
  • Storage Diseases, Copper
  • Westphal-Strumpell Syndromes
  • Pseudosclerotic type of Wilson's disease
  • Storage Disease, Copper
  • Degeneration, Progressive Lenticular
  • Lenticular Degeneration, Progressive
  • Westphal-Strumpell form of Wilson's disease
  • disease wilson
  • Degeneration, Hepatolenticular
  • Kinnier-Wilson Diseases
  • Hepato Neurologic Wilson Disease
  • Wilson's disease (disorder)
  • Diseases, Hepato-Neurologic Wilson
  • Hepato-Neurologic Wilson Disease
Frequently Asked Questions
What is the ICD-10 code for wilson's disease?

The ICD-10-CM code for wilson's disease is E83.01. The full clinical description is "Wilson's disease". E83.01 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E83.01 mean?

ICD-10-CM code E83.01 represents “Wilson's disease”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.

Is E83.01 a billable code?

Yes, E83.01 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E83.01 in?

E83.01 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E83.01?

E83.01 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 6 more.

What SNOMED CT codes does E83.01 map to?

E83.01 maps to 12 SNOMED CT concepts: 724766009, 722966004, 1259619002, 79886009, 88518009, and 7 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E83.01?

E83.01 is linked to 1 UMLS Concept Unique Identifier: C0019202. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E83.01 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like wilson's disease affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of E83.01?

There is no direct ICD-11 mapping available for E83.01 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.