E74.05
BillableLysosome-associated membrane protein 2 [LAMP2] deficiency
Lysosome-associated membrane protein 2 [LAMP2] deficiency
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Danon disease
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •transitory endocrine and metabolic disorders specific to newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- •diabetes mellitusE08-E13
- •hypoglycemia NOSE16.2
- •increased secretion of glucagonE16.3
- •mucopolysaccharidosisE76.0-E76.3
Code Also
A second code may be required; sequencing depends on circumstances
- , if applicable, associated manifestations such as:
- •dilated cardiomyopathyI42.0
- •obstructive hypertrophic cardiomyopathyI42.1
Related Codes(6)
Also Known As / Clinical Terms(74)
UMLS
- ANTOPOL DISEASEC0878677
- Antopol DiseaseC0878677
- Cardiomyopathies, Glycogen StorageC0878677
- Cardiomyopathy, Glycogen StorageC0878677
- DANON DISEASEC0878677
- Danon DiseaseC0878677
- Danon diseaseC0878677
- Disease, AntopolC0878677
- GLYCOGEN STORAGE DISEASE IIbC0878677
- GSD IIb, FORMERLYC0878677
- GSD2B, FORMERLYC0878677
- Glycogen Storage CardiomyopathiesC0878677
- Glycogen Storage CardiomyopathyC0878677
- Glycogen Storage Disease IIbC0878677
- Glycogen Storage Disease Limited to the HeartC0878677
- Glycogen Storage Disease Type 2BC0878677
- Glycogen Storage Disease Type IIbC0878677
- Glycogen storage disease due to LAMP-2 deficiencyC0878677
- Glycogen storage disease due to lysosomal associated membrane protein 2 deficiencyC0878677
- Glycogen storage disease due to lysosomal associated membrane protein 2 deficiency (disorder)C0878677
- Glycogen storage disease type 2BC0878677
- Glycogen storage disease type IIbC0878677
- Glycogenosis due to LAMP-2 deficiencyC0878677
- LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY, FORMERLYC0878677
- Lysosomal Glycogen Storage Disease with Normal Acid MaltaseC0878677
- Lysosomal Glycogen Storage Disease without Acid Maltase DeficiencyC0878677
- Lysosomal glycogen storage disease with normal acid maltaseC0878677
- Lysosomal glycogen storage disease with normal acid maltase activityC0878677
- Lysosomal glycogen storage disease without acid maltase deficiencyC0878677
- Lysosome-associated membrane protein 2 (LAMP2) deficiencyC0878677
- Lysosome-associated membrane protein 2 [LAMP2] deficiencyC0878677
- PSEUDOGLYCOGENOSIS IIC0878677
- Pseudoglycogenosis 2C0878677
- Pseudoglycogenosis 2sC0878677
- Pseudoglycogenosis IIC0878677
- Pseudoglycogenosis IIsC0878677
- VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKEDC0878677
- Vacuolar Cardiomyopathy and Myopathy, X linkedC0878677
- Vacuolar Cardiomyopathy and Myopathy, X-linkedC0878677
- X Linked Vacuolar Cardiomyopathy and MyopathyC0878677
- X-Linked Vacuolar Cardiomyopathy and MyopathyC0878677
- X-linked pseudoglycogenosis IIC0878677
- X-linked vacuolar cardiomyopathy and myopathyC0878677
Clinical Terms
- Pseudoglycogenosis IIs
- Pseudoglycogenosis 2s
- Glycogen Storage Disease Type 2B
- Glycogen Storage Disease IIb
- PSEUDOGLYCOGENOSIS II
- X-linked pseudoglycogenosis II
- DANON DISEASE
- LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY, FORMERLY
- Cardiomyopathy, Glycogen Storage
- Disease, Antopol
- Glycogen storage disease due to lysosomal associated membrane protein 2 deficiency
- VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED
- GSD2B, FORMERLY
- Glycogen Storage Cardiomyopathies
- X-Linked Vacuolar Cardiomyopathy and Myopathy
- Glycogen Storage Disease Type IIb
- Glycogen storage disease due to LAMP-2 deficiency
- Lysosomal glycogen storage disease with normal acid maltase activity
- Lysosomal glycogen storage disease without acid maltase deficiency
- ANTOPOL DISEASE
- Glycogen Storage Cardiomyopathy
- X Linked Vacuolar Cardiomyopathy and Myopathy
- Cardiomyopathies, Glycogen Storage
- Lysosomal glycogen storage disease with normal acid maltase
- Glycogen storage disease due to lysosomal associated membrane protein 2 deficiency (disorder)
- Pseudoglycogenosis 2
- Lysosome-associated membrane protein 2 (LAMP2) deficiency
- Glycogenosis due to LAMP-2 deficiency
- Vacuolar Cardiomyopathy and Myopathy, X linked
- GSD IIb, FORMERLY
- Glycogen Storage Disease Limited to the Heart
Frequently Asked Questions
What is the ICD-10 code for lysosome-associated membrane protein 2 [lamp2] deficiency?
The ICD-10-CM code for lysosome-associated membrane protein 2 [lamp2] deficiency is E74.05. The full clinical description is "Lysosome-associated membrane protein 2 [LAMP2] deficiency". E74.05 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E74.05 mean?
ICD-10-CM code E74.05 represents “Lysosome-associated membrane protein 2 [LAMP2] deficiency”. 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 E74.05 a billable code?
Yes, E74.05 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E74.05 in?
E74.05 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E74.05?
E74.05 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 7 more.
What are the UMLS CUIs for E74.05?
E74.05 is linked to 1 UMLS Concept Unique Identifier: C0878677. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E74.05 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like lysosome-associated membrane protein 2 [lamp2] deficiency 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 E74.05?
There is no direct ICD-11 mapping available for E74.05 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.