E83.01
BillableWilson's disease
Wilson's disease
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- dietary mineral deficiency (E58-E61)
- parathyroid disorders (E20-E21)
- vitamin D deficiency (E55.-)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Code Also
A second code may be required; sequencing depends on circumstances
- associated Kayser Fleischer ring (H18.04-)
Also Known As / Clinical Terms
SNOMED CT
- Copper metabolism disorder79886009
- Disorder of copper metabolism79886009
- Copper storage disease88518009
- Hepatocerebral degeneration88518009
- Hepatolenticular degeneration88518009
- Hepatolenticular degeneration syndrome88518009
- Kinnier-Wilson disease88518009
- Neurohepatic degeneration88518009
- Progressive lenticular degeneration88518009
- WD - Wilson's disease88518009
- Wilson disease88518009
- Wilson's disease88518009
- Pseudosclerotic type of Wilson's disease190823004
- Westphal-Strumpell cerebral pseudosclerosis190823004
- Westphal-Strumpell form of Wilson's disease190823004
- Westphal-Strumpell syndrome190823004
- Chorea due to heredodegenerative disorder722966004
- Dementia due to metabolic abnormality722979008
- Chorea co-occurrent and due to Wilson disease724766009
- Chorea with Wilson disease724766009
- Disorder of liver due to disorder of mineral metabolism737204007
- Hypoparathyroidism due to Wilson disease1186797002
- Dementia due to genetic disease1259476008
- Dementia due to Wilson disease1259511006
- Dementia due to Wilson's disease1259511006
- Dementia due to hepatolenticular degeneration1259511006
- Chorea due to metabolic disorder1259619002
- Dystonia due to Wilson disease1263524000
UMLS
- Cerebral PseudosclerosesC0019202
- Cerebral PseudosclerosisC0019202
- Copper Storage DiseaseC0019202
- Copper Storage DiseasesC0019202
- Copper storage diseaseC0019202
- Degeneration Syndrome, HepatolenticularC0019202
- Degeneration Syndromes, HepatolenticularC0019202
- Degeneration, HepatocerebralC0019202
- Degeneration, HepatolenticularC0019202
- Degeneration, NeurohepaticC0019202
- Degeneration, Progressive LenticularC0019202
- Degenerations, HepatocerebralC0019202
- Degenerations, NeurohepaticC0019202
- Disease, Copper StorageC0019202
- Diseases, Copper StorageC0019202
- Diseases, Hepato-Neurologic WilsonC0019202
- Diseases, Kinnier-WilsonC0019202
- Gowers' choreaC0019202
- HEPATOLENTICULAR DEGENERATIONC0019202
- HEPATONEUROLOGIC WILSON DISC0019202
- Hepato Neurologic Wilson DiseaseC0019202
- Hepato-Neurologic Wilson DiseaseC0019202
- Hepato-Neurologic Wilson DiseasesC0019202
- Hepato-lenticular degenerationC0019202
- Hepatocerebral DegenerationC0019202
- Hepatocerebral DegenerationsC0019202
- Hepatocerebral degenerationC0019202
- Hepatolenticular DegenerationC0019202
- Hepatolenticular Degeneration SyndromeC0019202
- Hepatolenticular Degeneration SyndromesC0019202
- Hepatolenticular degenerationC0019202
- Hepatolenticular degeneration syndromeC0019202
- KINNIER WILSON DISC0019202
- Kinnier Wilson DiseaseC0019202
- Kinnier-Wilson DiseaseC0019202
- Kinnier-Wilson DiseasesC0019202
- Kinnier-Wilson diseaseC0019202
- Lenticular Degeneration, ProgressiveC0019202
- Neurohepatic DegenerationC0019202
- Neurohepatic DegenerationsC0019202
- Neurohepatic degenerationC0019202
- Progressive Lenticular DegenerationC0019202
- Progressive lenticular degenerationC0019202
- Pseudoscleroses, CerebralC0019202
- PseudosclerosisC0019202
- Pseudosclerosis, CerebralC0019202
- Pseudosclerotic type of Wilson's diseaseC0019202
- Storage Disease, CopperC0019202
- Storage Diseases, CopperC0019202
- Syndrome, Hepatolenticular DegenerationC0019202
- Syndromes, Hepatolenticular DegenerationC0019202
- WD - Wilson's diseaseC0019202
- WILSON DISC0019202
- WILSON DISEASEC0019202
- WILSONS DISC0019202
- WNDC0019202
- Westphal Strumpell SyndromeC0019202
- Westphal Strumpell diseaseC0019202
- Westphal pseudosclerosisC0019202
- Westphal-Strumpell SyndromeC0019202
- Westphal-Strumpell SyndromesC0019202
- Westphal-Strumpell cerebral pseudosclerosisC0019202
- Westphal-Strumpell form of Wilson's diseaseC0019202
- Westphal-Strumpell syndromeC0019202
- Westphal-Strumpell syndrome (disorder)C0019202
- Wilson DiseaseC0019202
- Wilson Disease, Hepato-NeurologicC0019202
- Wilson Diseases, Hepato-NeurologicC0019202
- Wilson diseaseC0019202
- Wilson's DiseaseC0019202
- Wilson's diseaseC0019202
- Wilson's disease (disorder)C0019202
- Wilsons DiseaseC0019202
- cerebral pseudosclerosisC0019202
- disease wilsonC0019202
- disease wilson'sC0019202
- disease wilsonsC0019202
- diseases wilsonC0019202
- familial hepatitisC0019202
- hepato-lenticular degenerationC0019202
- hepatocerebral degenerationC0019202
- hepatolenticular degenerationC0019202
- neurohepatic degenerationC0019202
- wilson diseaseC0019202
- wilson's diseaseC0019202
- wilsons diseaseC0019202
Frequently Asked Questions
What is ICD-10 code E83.01?
ICD-10-CM code E83.01 represents "Wilson's disease". It 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.
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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.