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 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
- 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
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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.