E74.09
BillableOther glycogen storage disease
Other glycogen storage disease
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Andersen disease
- Glycogen storage disease, types 0, IV, VI-XI
- Hers disease
- Liver phosphorylase deficiency
- Muscle phosphofructokinase deficiency
- Tauri 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, hepatic form6075009
- 1,4,alpha-glucan 6-alpha-glucosyltransferase deficiency11179002
- Amylopectinosis11179002
- Andersen disease11179002
- Andersen's disease11179002
- Brancher deficiency glycogen storage disease11179002
- Branching enzyme deficiency11179002
- Branching-transferase deficiency glycogenosis11179002
- GSD IV11179002
- Glycogen storage disease type IV11179002
- Glycogen storage disease, type 411179002
- Glycogen storage disease, type IV11179002
- Glycogenosis, type 411179002
- Glycogen storage disease, muscular form15978003
- GSD VI29291001
- Glycogen storage disease, type VI29291001
- Hepatic glycogen phosphorylase deficiency29291001
- Hepatic phosphorylase deficiency29291001
- Hers disease29291001
- GSD VIII41527003
- Glycogen storage disease type 841527003
- Glycogen storage disease type VIII41527003
- Glycogenosis due to inactive hepatic glycogen phosphorylase41527003
- Glycogenosis due to inactive phosphorylase41527003
- Fanconi-Bickel syndrome61598006
- Glycogenosis with glucoaminophosphaturia61598006
- Hepatic glycogenosis with de Toni-Debre-Fanconi syndrome61598006
- Hepatic glycogenosis with de Toni-Debré-Fanconi syndrome61598006
- Pseudo-phlorizin diabetes61598006
- Renal glucose-losing syndrome61598006
- GSD VII89597008
- Glycogen storage disease, type 789597008
- Glycogen storage disease, type VII89597008
- Muscle phosphofructokinase deficiency89597008
- Tarui's disease89597008
- Glycogen phosphorylase kinase deficiency235908005
- Glycogen storage disease type IX235908005
- Glycogenosis viiia235908005
- Hepatic phosphorylase kinase deficiency235908005
- PHK - Hepatic phosphorylase kinase deficiency235908005
- Phosphorylase kinase deficiency of liver235908005
- Glycogen storage disease type 0237964009
- Glycogen synthase deficiency237964009
- Glycogen storage disease type Ic237965005
- Phosphate transport defect237965005
- Glycogen phosphorylase kinase deficiency, autosomal recessive297252005
- Cardiac glycogen phosphorylase kinase deficiency297253000
- Hepatic and muscle glycogen phosphorylase kinase deficiency297254006
- Hepatic glycogen phosphorylase kinase deficiency297255007
- Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase367406009
- Danon disease419097006
- Glycogen storage disease due to LAMP-2 deficiency419097006
- Glycogen storage disease due to lysosomal associated membrane protein 2 deficiency419097006
- Glycogenosis due to LAMP-2 deficiency419097006
- Lysosomal glycogen storage disease with normal acid maltase activity419097006
- Adult polyglucosan body disease721099001
- Polyglucosan body disease adult form721099001
- Glycogen storage disease due to hepatic glycogen synthase deficiency725026008
- Glycogen storage disease due to liver glycogen synthase deficiency725026008
- Glycogen storage disease type 0a725026008
- Glycogenosis type 0a725026008
- Hepatic glycogen synthase deficiency725026008
- Glycogen storage disease due to muscle and heart glycogen synthase deficiency725027004
- Glycogen storage disease type 0b725027004
- Glycogenosis due to muscle and heart glycogen synthase deficiency725027004
- Glycogenosis type 0b725027004
- Muscle and heart glycogen synthase deficiency725027004
- PGBM1 - polyglucosan body myopathy type 1774148007
- Polyglucosan body myopathy type 1774148007
- Glycogen storage disease due to muscle phosphorylase kinase deficiency819953000
- Glycogen storage disease type 9D819953000
- Glycogen storage disease type IXd819953000
- Glycogenosis type 9D819953000
- Cardiomyopathy due to storage disease860839005
- Glycogen storage disease due to muscle pyruvate kinase deficiency860858001
- Glycogen storage disease due to liver and muscle glycogen phosphorylase kinase deficiency860860004
- Glycogen storage disease type IXB860860004
- Glycogen storage disease with hypertrophic cardiomyopathy871638006
- Hypertrophic cardiomyopathy due to glycogen storage disease871638006
- GSDXIII - glycogen storage disease type XIII1162916008
- Glycogen storage disease due to muscle beta-enolase deficiency1162916008
- Glycogenosis due to muscle beta-enolase deficiency1162916008
- Glycogenosis type 131162916008
- Muscle enolase deficiency1162916008
- Glycogen storage disease due to lactate dehydrogenase deficiency1186809004
- Glycogen storage disease type XI1186809004
- Glycogen storage disease due to aldolase A deficiency1187461004
- Glycogen storage disease type 121187461004
- Glycogen storage disease type XII1187461004
- Glycogenosis due to aldolase A deficiency1187461004
- Glycogenosis type 121187461004
- Glycogenosis type XII1187461004
- Glycogen storage disease due to phosphoglycerate kinase 1 deficiency1187462006
- Glycogenosis due to phosphoglycerate kinase 1 deficiency1187462006
- PGBM2 - polyglucosan body myopathy type 21228849007
- Polyglucosan body myopathy type 21228849007
UMLS
- 1,4,alpha-glucan 6-alpha-glucosyltransferase deficiencyC0017923
- AMYLOPECTINOSISC0017923
- ANDERSEN DISC0017923
- ANDERSEN DISEASEC0017923
- ANDERSENS DISC0017923
- AmylopectinosesC0017923
- AmylopectinosisC0017923
- Andersen DiseaseC0017923
- Andersen diseaseC0017923
- Andersen glycogenosisC0017923
- Andersen's DiseaseC0017923
- Andersen's diseaseC0017923
- Andersens DiseaseC0017923
- BRANCHER DEFICC0017923
- BRANCHER DEFICIENCYC0017923
- Brancher DeficienciesC0017923
- Brancher DeficiencyC0017923
- Brancher deficiencyC0017923
- Brancher deficiency glycogen storage diseaseC0017923
- Branching enzyme deficiencyC0017923
- Branching-transferase deficiency glycogenosisC0017923
- DEFIC BRANCHERC0017923
- Deficiencies, BrancherC0017923
- Deficiencies, Gbe1C0017923
- Deficiency of 1,4-alpha-glucan branching enzymeC0017923
- Deficiency of 1,4-alpha-glucan branching enzyme (disorder)C0017923
- Deficiency of amylo-(1,4,6)-transglycosylaseC0017923
- Deficiency of branching enzymeC0017923
- Deficiency, BrancherC0017923
- Deficiency, Gbe1C0017923
- Disease, AndersenC0017923
- Disease, Andersen'sC0017923
- GBE1 DEFICIENCYC0017923
- GLYCOGEN BRANCHING ENZYME DEFICIENCYC0017923
- GLYCOGEN STORAGE DIS IVC0017923
- GLYCOGEN STORAGE DISEASE IVC0017923
- GLYCOGENOSIS IVC0017923
- GSD IVC0017923
- GSD type IVC0017923
- GSD4C0017923
- Gbe1 DeficienciesC0017923
- Gbe1 DeficiencyC0017923
- Glycogen Branching Enzyme DeficiencyC0017923
- Glycogen Storage Disease Type 4C0017923
- Glycogen Storage Disease Type IVC0017923
- Glycogen branching enzyme deficiencyC0017923
- Glycogen storage disease IVC0017923
- Glycogen storage disease type 4C0017923
- Glycogen storage disease type IVC0017923
- Glycogen storage disease, type 4C0017923
- Glycogen storage disease, type IVC0017923
- Glycogen storage disease, type IV (disorder)C0017923
- Glycogenoses, Type IVC0017923
- Glycogenosis 4C0017923
- Glycogenosis 4sC0017923
- Glycogenosis IVC0017923
- Glycogenosis IVsC0017923
- Glycogenosis type IVC0017923
- Glycogenosis, Type IVC0017923
- Glycogenosis, type 4C0017923
- Glycogenosis, type IVC0017923
- Type IV GlycogenosesC0017923
- Type IV GlycogenosisC0017923
- Type IV glycogenosisC0017923
- amylopectinosisC0017923
- andersen diseaseC0017923
- andersen's diseaseC0017923
- brancher deficiencyC0017923
- brancher deficiency glycogenosisC0017923
- brancher glycogen storage diseaseC0017923
- glycogen storage disease type IVC0017923
- glycogen storage disease type ivC0017923
- glycogenosis type 4C0017923
- glycogenosis type IVC0017923
- glycogenosis type ivC0017923
- gsd ivC0017923
- type iv glycogen storage diseaseC0017923
- DEFIC MUSCLE PHOSPHOFRUCTOKINASEC0017926
- Deficiencies, Muscle PhosphofructokinaseC0017926
- Deficiencies, PfkmC0017926
- Deficiency, Muscle PhosphofructokinaseC0017926
- Deficiency, PfkmC0017926
- Disease, TaruiC0017926
- Disease, Tarui'sC0017926
- GLYCOGEN STORAGE DIS VIIC0017926
- GLYCOGEN STORAGE DISEASE VIIC0017926
- GSD VIIC0017926
- GSD7C0017926
- GSDVIIC0017926
- Glycogen Storage Disease Type VIIC0017926
- Glycogen Storage Disease VIIC0017926
- Glycogen storage disease type VIIC0017926
- Glycogen storage disease, type 7C0017926
- Glycogen storage disease, type VIIC0017926
- Glycogen storage disease, type VII (disorder)C0017926
- Glycogenosis 7C0017926
- Glycogenosis type VIIC0017926
- MUSCLE PHOSPHOFRUCTOKINASE DEFICC0017926
- MUSCLE PHOSPHOFRUCTOKINASE DEFICIENCYC0017926
- Muscle Phosphofructokinase DeficienciesC0017926
- Muscle Phosphofructokinase DeficiencyC0017926
- Muscle phosphofructokinase deficiencyC0017926
- PFKM DEFICIENCYC0017926
- PFKM DeficiencyC0017926
- PFKM deficiencyC0017926
- Pfkm DeficienciesC0017926
- Pfkm DeficiencyC0017926
- Phosphofructokinase Deficiencies, MuscleC0017926
- Phosphofructokinase DeficiencyC0017926
- Phosphofructokinase Deficiency, MuscleC0017926
- Phosphofructokinase deficiencyC0017926
- TARUI DISC0017926
- TARUI DISEASEC0017926
- TARUIS DISC0017926
- Tarui DiseaseC0017926
- Tarui diseaseC0017926
- Tarui's DiseaseC0017926
- Tarui's diseaseC0017926
- Taruis DiseaseC0017926
- Tauri diseaseC0017926
- disease taruiC0017926
- diseases tarui'sC0017926
- glycogen storage disease type VIIC0017926
- glycogenosis type VIIC0017926
- gsd viiC0017926
- muscle phosphofructokinase deficiencyC0017926
- phosphofructokinase deficiencyC0017926
- phosphofructokinase myopathyC0017926
- tarui diseaseC0017926
- tarui's diseaseC0017926
- taruis diseaseC0017926
- tauri diseaseC0017926
- Disease, HersC0017925
- Disease, Hers'C0017925
- GLYCOGEN STORAGE DIS VIC0017925
- GLYCOGEN STORAGE DISEASE VIC0017925
- GSD VIC0017925
- GSD type VIC0017925
- GSD6C0017925
- Glycogen Storage Disease Type VIC0017925
- Glycogen storage disease type VIC0017925
- Glycogen storage disease, type VIC0017925
- Glycogen storage disease, type VI (disorder)C0017925
- Glycogenosis 6C0017925
- Glycogenosis Type VIC0017925
- Glycogenosis VIC0017925
- Glycogenosis type VIC0017925
- HERS DISC0017925
- HERS DISEASEC0017925
- Hepatic Glycogen Phosphorylase DeficiencyC0017925
- Hepatic glycogen phosphorylase deficiencyC0017925
- Hepatic phosphorylase deficiencyC0017925
- Her DiseaseC0017925
- Hers DiseaseC0017925
- Hers diseaseC0017925
- Hers glycogenosisC0017925
- Hers' DiseaseC0017925
- Hers' diseaseC0017925
- Liver Phosphorylase Deficiency SyndromeC0017925
- Liver phosphorylase deficiencyC0017925
- Liver phosphorylase deficiency syndromeC0017925
- PHOSPHORYLASE DEFICIENCY GLYCOGEN-STORAGE DISEASE OF LIVERC0017925
- Type VI, GlycogenosisC0017925
- glycogen storage disease type VIC0017925
- glycogenosis type VIC0017925
- hepatic phosphorylase deficiencyC0017925
- hepatophosphorylase deficiency glycogenosisC0017925
- her's diseaseC0017925
- hers diseaseC0017925
- liver phosphorylase deficiencyC0017925
- Glycogen storage disease, types 0, IV, VI-XIC2874266
- Other glycogen storage diseaseC2874267
Frequently Asked Questions
What is the ICD-10 code for other glycogen storage disease?
The ICD-10-CM code for other glycogen storage disease is E74.09. The full clinical description is "Other glycogen storage disease". E74.09 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E74.09 mean?
ICD-10-CM code E74.09 represents "Other glycogen storage 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 E74.09 a billable code?
Yes, E74.09 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E74.09 in?
E74.09 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E74.09?
E74.09 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 E74.09 map to?
E74.09 maps to 30 SNOMED CT concepts: 11179002, 721099001, 297253000, 860839005, 419097006, and 25 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E74.09?
E74.09 is linked to 5 UMLS Concept Unique Identifiers: C0017923, C0017926, C0017925, C2874266, C2874267. 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.