E76

The ICD-10-CM code for disorders of glycosaminoglycan metabolism is E76. The full clinical description is "Disorders of glycosaminoglycan metabolism". E76 is a non-billable header code. Use a more specific child code for billing purposes.

ICD-10-CM code E76 represents “Disorders of glycosaminoglycan metabolism”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a non-billable header code. Use a more specific child code for billing purposes.

No, E76 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 6 child codes under E76.

E76 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

E76 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 3 more.

E76 has 6 child codes, including: E76.0 (Mucopolysaccharidosis, type I), E76.1 (Mucopolysaccharidosis, type II), E76.2 (Other mucopolysaccharidoses), E76.3 (Mucopolysaccharidosis, unspecified), and 2 more.

E76 is linked to 1 UMLS Concept Unique Identifier: C0342837. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like disorders of glycosaminoglycan metabolism 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.

E76 maps to the ICD-11 code: 5C56.3Z (Mucopolysaccharidosis, unspecified).