E74.03
BillableCori disease
Cori disease
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Forbes disease
- Type III 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(152)
SNOMED CT
- Glycogen storage disease, hepatic form6075009
- Glycogen storage disease, muscular form15978003
- Amylo-1,6-glucosidase deficiency66937008
- Cori disease66937008
- Cori's disease66937008
- Debrancher deficiency glycogen storage disease66937008
- Debrancher enzyme deficiency66937008
- GSD III66937008
- Glycogen storage disease type 366937008
- Glycogen storage disease type III66937008
- Glycogen storage disease, type III66937008
- Limit dextrin - glycogen66937008
- Limit dextrinosis66937008
- Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis829973009
- Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis due to HOIL-1 deficiency1365687001
- Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis due to HOIP deficiency1365687001
- Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis due to RNF31 mutation1365687001
UMLS
- AGL DEFICIENCYC0017922
- AGL deficiencyC0017922
- AMYLO-1,6-GLUCOSIDASE DEFICIENCYC0017922
- Amylo 1,6 Glucosidase DeficiencyC0017922
- Amylo-1,6-Glucosidase DeficienciesC0017922
- Amylo-1,6-Glucosidase DeficiencyC0017922
- Amylo-1,6-glucosidase deficiencyC0017922
- CORI DISC0017922
- CORI DISEASEC0017922
- CORIS DISC0017922
- Cori DiseaseC0017922
- Cori diseaseC0017922
- Cori's DiseaseC0017922
- Cori's diseaseC0017922
- Coris DiseaseC0017922
- DEBRANCHER DEFICC0017922
- DEFIC DEBRANCHERC0017922
- Debrancher DeficienciesC0017922
- Debrancher Deficiencies, GlycogenC0017922
- Debrancher DeficiencyC0017922
- Debrancher Deficiency, GlycogenC0017922
- Debrancher deficiencyC0017922
- Debrancher deficiency glycogen storage diseaseC0017922
- Debrancher enzyme deficiencyC0017922
- Deficiencies, Amylo-1,6-GlucosidaseC0017922
- Deficiencies, DebrancherC0017922
- Deficiencies, Glycogen DebrancherC0017922
- Deficiency, Amylo-1,6-GlucosidaseC0017922
- Deficiency, DebrancherC0017922
- Deficiency, Glycogen DebrancherC0017922
- Dextrinoses, LimitC0017922
- Dextrinosis, LimitC0017922
- Disease, CoriC0017922
- Disease, Cori'sC0017922
- Disease, ForbesC0017922
- FORBES DISC0017922
- FORBES DISEASEC0017922
- Forbes DiseaseC0017922
- Forbes diseaseC0017922
- Forbes' diseaseC0017922
- GDE DEFICIENCYC0017922
- GLYCOGEN DEBRANCHER DEFICIENCYC0017922
- GLYCOGEN DEBRANCHING ENZYME DEFICC0017922
- GLYCOGEN STORAGE DIS IIIC0017922
- GLYCOGEN STORAGE DISEASE IIIC0017922
- GSD IIIC0017922
- GSD3C0017922
- Glycogen Debrancher DeficienciesC0017922
- Glycogen Debrancher DeficiencyC0017922
- Glycogen Debranching Enzyme DeficiencyC0017922
- Glycogen Storage Disease IIIC0017922
- Glycogen Storage Disease Type 3C0017922
- Glycogen Storage Disease Type IIIC0017922
- Glycogen debrancher deficiencyC0017922
- Glycogen storage disease type 3C0017922
- Glycogen storage disease type IIIC0017922
- Glycogen storage disease, type IIIC0017922
- Glycogen storage disease, type III (disorder)C0017922
- Glycogenosis 3C0017922
- Glycogenosis 3sC0017922
- LIMIT DEXTRINOSISC0017922
- Limit DextrinosesC0017922
- Limit DextrinosisC0017922
- Limit dextrin - glycogenC0017922
- Limit dextrinosisC0017922
- Type III glycogen storage diseaseC0017922
- amylo 1,6 glucosidase deficiencyC0017922
- cori diseaseC0017922
- cori's diseaseC0017922
- debrancher deficiencyC0017922
- debrancher enzyme deficiencyC0017922
- debrancher glycogen storage diseaseC0017922
- forbes diseaseC0017922
- forbes' diseaseC0017922
- glycogen storage disease iiiC0017922
- glycogen storage disease type IIIC0017922
- glycogenosis type IIIC0017922
- limit dextrinosisC0017922
Clinical Terms
- debrancher glycogen storage disease
- Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis due to HOIP deficiency
- Limit dextrinosis
- Debrancher Deficiencies
- glycogen storage disease iii
- Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis
- Disease, Forbes
- Debrancher Deficiencies, Glycogen
- Glycogenosis 3s
- DEBRANCHER DEFIC
- Debrancher Deficiency, Glycogen
- debrancher enzyme deficiency
- Amylo-1,6-Glucosidase Deficiency
- Forbes Disease
- DEFIC DEBRANCHER
- Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis due to HOIL-1 deficiency
- FORBES DIS
- Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis due to RNF31 mutation
- Dextrinosis, Limit
- GLYCOGEN DEBRANCHER DEFICIENCY
- CORI DIS
- Dextrinoses, Limit
- amylo 1,6 glucosidase deficiency
- glycogenosis type III
- Debrancher Deficiency
- Glycogen storage disease, muscular form
- AGL DEFICIENCY
- Forbes' disease
- Limit Dextrinoses
- Deficiency, Amylo-1,6-Glucosidase
- Glycogen storage disease type 3
- Deficiencies, Debrancher
- Type III glycogen storage disease
- Deficiency, Debrancher
- glycogen storage disease type III
- GLYCOGEN STORAGE DIS III
- GLYCOGEN DEBRANCHING ENZYME DEFIC
- Deficiencies, Glycogen Debrancher
- Cori's Disease
- CORIS DIS
- Deficiencies, Amylo-1,6-Glucosidase
- GSD3
- Glycogen storage disease, hepatic form
- Glycogen Debrancher Deficiencies
- GDE DEFICIENCY
- Glycogen storage disease, type III (disorder)
- Glycogen Debranching Enzyme Deficiency
- Deficiency, Glycogen Debrancher
- GSD III
- Disease, Cori's
- Limit dextrin - glycogen
- Glycogenosis 3
- Debrancher deficiency glycogen storage disease
- Amylo-1,6-Glucosidase Deficiencies
- Disease, Cori
- Glycogen storage disease, type III
- Coris Disease
Frequently Asked Questions
What is the ICD-10 code for cori disease?
The ICD-10-CM code for cori disease is E74.03. The full clinical description is "Cori disease". E74.03 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E74.03 mean?
ICD-10-CM code E74.03 represents “Cori 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 E74.03 a billable code?
Yes, E74.03 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E74.03 in?
E74.03 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E74.03?
E74.03 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 E74.03 map to?
E74.03 maps to 5 SNOMED CT concepts: 66937008, 829973009, 1365687001, 6075009, 15978003. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E74.03?
E74.03 is linked to 1 UMLS Concept Unique Identifier: C0017922. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E74.03 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like cori 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 E74.03?
There is no direct ICD-11 mapping available for E74.03 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.