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 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)
- diabetes mellitus (E08-E13)
- hypoglycemia NOS (E16.2)
- increased secretion of glucagon (E16.3)
- mucopolysaccharidosis (E76.0-E76.3)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
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
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.
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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.