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 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
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
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.
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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.