E75.28
BillableCanavan disease
Canavan 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)
- mucolipidosis, types I-III (E77.0-E77.1)
- Refsum's disease (G60.1)
- adrenoleukodystrophy [Addison-Schilder] (E71.528)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
UMLS
- ACY2 DEFICIENCYC0206307
- AMINOACYLASE 2 DEFICIENCYC0206307
- ASP DEFICIENCYC0206307
- ASPA DEFICIENCYC0206307
- ASPARTOACYLASE DEFICIENCYC0206307
- Aspartoacylase deficiencyC0206307
- CANAVAN DISEASEC0206307
- CANAVAN-VAN BOGAERT-BERTRAND DISEASEC0206307
- Canavan DiseaseC0206307
- Canavan diseaseC0206307
- Canavan van Bogaert Bertrand DiseaseC0206307
- Canavan's diseaseC0206307
- Canavan-van Bogaert-Bertrand DiseaseC0206307
- Canavan-van Bogaert-Bertrand diseaseC0206307
- Canavan-van-Bogaert-Bertrand diseaseC0206307
- Disease, CanavanC0206307
- Disease, Canavan-van Bogaert-BertrandC0206307
- Disease, Von Bogaert-BertrandC0206307
- Leukodystrophy, SpongiformC0206307
- SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEMC0206307
- Spongiform LeukodystrophyC0206307
- Spongiform leucodystrophyC0206307
- Spongy Degeneration Of Central Nervous SystemC0206307
- Spongy Degeneration of InfancyC0206307
- Spongy Degeneration of White Matter In InfancyC0206307
- Spongy Degeneration of the BrainC0206307
- Spongy Degeneration of the Central Nervous SystemC0206307
- Spongy Disease of Central Nervous SystemC0206307
- Spongy Disease of White MatterC0206307
- Spongy degeneration of central nervous systemC0206307
- Spongy degeneration of central nervous system (disorder)C0206307
- Spongy degeneration of white matterC0206307
- Spongy degeneration of white matter in infancyC0206307
- Syndrome, Van Bogaert-BertrandC0206307
- Van Bogaert Bertrand SyndromeC0206307
- Van Bogaert-Bertrand SyndromeC0206307
- Von Bogaert Bertrand DiseaseC0206307
- Von Bogaert-Bertrand DiseaseC0206307
- canavan diseaseC0206307
- canavan's diseaseC0206307
- canavans diseaseC0206307
Frequently Asked Questions
What is the ICD-10 code for canavan disease?
The ICD-10-CM code for canavan disease is E75.28. The full clinical description is "Canavan disease". E75.28 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E75.28 mean?
ICD-10-CM code E75.28 represents "Canavan 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 E75.28 a billable code?
Yes, E75.28 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E75.28 in?
E75.28 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E75.28?
E75.28 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 are the UMLS CUIs for E75.28?
E75.28 is linked to 1 UMLS Concept Unique Identifier: C0206307. 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.