E74.04
BillableMcArdle disease
McArdle disease
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Type V glycogen storage 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
Related Codes(6)
Also Known As / Clinical Terms(127)
SNOMED CT
- Glycogen storage disease, muscular form15978003
- GSD V55912009
- Glycogen storage disease type 555912009
- Glycogen storage disease type V55912009
- Glycogen storage disease, type V55912009
- Glycogenosis, type 555912009
- McArdle disease55912009
- McArdle's disease55912009
- Muscle glycogen phosphorylase deficiency55912009
- Myophosphorylase deficiency glycogenosis55912009
UMLS
- DEFIC MUSCLE PHOSPHORYLASEC0017924
- Deficiencies, Muscle PhosphorylaseC0017924
- Deficiencies, PYGMC0017924
- Deficiency, Muscle PhosphorylaseC0017924
- Deficiency, PYGMC0017924
- Disease, McArdleC0017924
- Disease, McArdle'sC0017924
- GLYCOGEN STORAGE DIS VC0017924
- GLYCOGEN STORAGE DISEASE VC0017924
- GSD VC0017924
- GSD type VC0017924
- GSD5C0017924
- Glycogen Storage Disease Type 5C0017924
- Glycogen Storage Disease Type VC0017924
- Glycogen Storage Disease VC0017924
- Glycogen storage disease type 5C0017924
- Glycogen storage disease type VC0017924
- Glycogen storage disease, type VC0017924
- Glycogen storage disease, type V (disorder)C0017924
- Glycogenosis 5C0017924
- Glycogenosis 5sC0017924
- Glycogenosis type VC0017924
- Glycogenosis, type 5C0017924
- MCARDLE DISC0017924
- MCARDLE DISEASEC0017924
- MCARDLES DISC0017924
- MUSCLE GLYCOGEN PHOSPHORYLASE DEFICIENCYC0017924
- MUSCLE PHOSPHORYLASE DEFICC0017924
- MYOPHOSPHORYLASE DEFICIENCYC0017924
- McArdle DiseaseC0017924
- McArdle Type Glycogen Storage DiseaseC0017924
- McArdle diseaseC0017924
- McArdle syndromeC0017924
- McArdle type glycogen storage diseaseC0017924
- McArdle's DiseaseC0017924
- McArdle's diseaseC0017924
- McArdles DiseaseC0017924
- McArdles diseaseC0017924
- Mcardle SyndromeC0017924
- Mcardle SyndromesC0017924
- Muscle Glycogen Phosphorylase DeficiencyC0017924
- Muscle Phosphorylase DeficienciesC0017924
- Muscle Phosphorylase DeficiencyC0017924
- Muscle glycogen phosphorylase deficiencyC0017924
- Muscle phosphorylase deficiencyC0017924
- Myophosphorylase deficienciesC0017924
- Myophosphorylase deficiencyC0017924
- Myophosphorylase deficiency glycogenosisC0017924
- PYGM DEFICIENCYC0017924
- PYGM DeficienciesC0017924
- PYGM DeficiencyC0017924
- PYGM deficiencyC0017924
- Phosphorylase Deficiencies, MuscleC0017924
- Phosphorylase Deficiency, MuscleC0017924
- Syndrome, McardleC0017924
- Syndromes, McardleC0017924
- Type V glycogen storage diseaseC0017924
- deficiencies, MyophosphorylaseC0017924
- deficiency, MyophosphorylaseC0017924
- disease mcardlesC0017924
- disease mcardles'sC0017924
- glycogen storage disease type VC0017924
- glycogen storage disease type vC0017924
- glycogenosis type VC0017924
- mcardle diseaseC0017924
- mcardle's diseaseC0017924
- mcardles diseaseC0017924
- muscle phosphorylase deficiencyC0017924
- myophosphorylase deficiencyC0017924
- type 5 glycogenosisC0017924
Clinical Terms
- GSD V
- Syndrome, Mcardle
- Glycogen storage disease type 5
- Myophosphorylase deficiencies
- Muscle glycogen phosphorylase deficiency
- Disease, McArdle
- MYOPHOSPHORYLASE DEFICIENCY
- deficiency, Myophosphorylase
- type 5 glycogenosis
- Glycogen storage disease, type V (disorder)
- MCARDLES DIS
- PYGM DEFICIENCY
- GLYCOGEN STORAGE DISEASE V
- Glycogen Storage Disease Type V
- McArdle syndrome
- Deficiency, PYGM
- McArdle type glycogen storage disease
- Deficiencies, PYGM
- Glycogenosis 5s
- Glycogen storage disease, muscular form
- Glycogenosis, type 5
- Muscle Phosphorylase Deficiencies
- disease mcardles
- Syndromes, Mcardle
- GSD5
- Phosphorylase Deficiency, Muscle
- MUSCLE PHOSPHORYLASE DEFIC
- Glycogenosis 5
- GLYCOGEN STORAGE DIS V
- McArdles Disease
- Mcardle Syndromes
- Muscle Phosphorylase Deficiency
- deficiencies, Myophosphorylase
- Glycogenosis type V
- Type V glycogen storage disease
- GSD type V
- Myophosphorylase deficiency glycogenosis
- mcardle's disease
- Phosphorylase Deficiencies, Muscle
- Deficiencies, Muscle Phosphorylase
- Disease, McArdle's
- Glycogen storage disease, type V
- MCARDLE DIS
- disease mcardles's
- Deficiency, Muscle Phosphorylase
- DEFIC MUSCLE PHOSPHORYLASE
- PYGM Deficiencies
Frequently Asked Questions
What is the ICD-10 code for mcardle disease?
The ICD-10-CM code for mcardle disease is E74.04. The full clinical description is "McArdle disease". E74.04 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E74.04 mean?
ICD-10-CM code E74.04 represents “McArdle 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 E74.04 a billable code?
Yes, E74.04 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E74.04 in?
E74.04 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E74.04?
E74.04 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 SNOMED CT codes does E74.04 map to?
E74.04 maps to 2 SNOMED CT concepts: 55912009, 15978003. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E74.04?
E74.04 is linked to 1 UMLS Concept Unique Identifier: C0017924. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E74.04 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like mcardle disease 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 E74.04?
There is no direct ICD-11 mapping available for E74.04 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.