E74.810
BillableGlucose transporter protein type 1 deficiency
Glucose transporter protein type 1 deficiency
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- De Vivo syndrome
- Glucose transport defect, blood-brain barrier
- Glut1 deficiency
- GLUT1 deficiency syndrome 1, infantile onset
- GLUT1 deficiency syndrome 2, childhood onset
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(2)
Also Known As / Clinical Terms(38)
UMLS
- De Vivo diseaseC1847501
- De Vivo syndromeC1847501
- Encephalopathy Due To Glut1 DeficiencyC1847501
- Encephalopathy due to GLUT1 deficiencyC1847501
- G1DC1847501
- GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERC1847501
- GLUT-1 deficiency syndromeC1847501
- GLUT1 DSC1847501
- GLUT1 deficiency syndromeC1847501
- GTPSC1847501
- Glucose Transporter Protein SyndromeC1847501
- Glucose Transporter Type 1 Deficiency SyndromeC1847501
- Glucose transport defect, blood-brain barrierC1847501
- Glucose transporter protein syndromeC1847501
- Glucose transporter protein type 1 deficiencyC1847501
- Glucose transporter type 1 deficiency syndromeC1847501
- Glucose transporter type1 (GLUT-1) deficiencyC1847501
- Glut1 Deficiency SyndromeC1847501
- Glut1 deficiencyC1847501
- GLUT1 deficiency syndrome 1, infantile onsetC5385209
- GLUT1 deficiency syndrome 2, childhood onsetC5385210
Clinical Terms
- Glucose Transporter Protein Syndrome
- Epilepsy due to glucose transporter protein type 1 deficiency syndrome
- Glucose Transporter Type 1 Deficiency Syndrome
- Glucose transporter type1 (GLUT-1) deficiency
- G1D
- Glucose transport defect, blood-brain barrier
- GLUT1 deficiency syndrome 1, infantile onset
- De Vivo syndrome
- GLUT1 deficiency syndrome
- GLUT-1 deficiency syndrome
- De Vivo disease
- Encephalopathy due to GLUT1 deficiency
- Glut1 deficiency
- GLUT1 deficiency syndrome 2, childhood onset
- GTPS
- GLUT1 DS
Frequently Asked Questions
What is the ICD-10 code for glucose transporter protein type 1 deficiency?
The ICD-10-CM code for glucose transporter protein type 1 deficiency is E74.810. The full clinical description is "Glucose transporter protein type 1 deficiency". E74.810 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E74.810 mean?
ICD-10-CM code E74.810 represents “Glucose transporter protein type 1 deficiency”. 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 E74.810 a billable code?
Yes, E74.810 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E74.810 in?
E74.810 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E74.810?
E74.810 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 E74.810 map to?
E74.810 maps to 1 SNOMED CT concept: 1260375002. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E74.810?
E74.810 is linked to 3 UMLS Concept Unique Identifiers: C1847501, C5385209, C5385210. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E74.810 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like glucose transporter protein type 1 deficiency 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 E74.810?
There is no direct ICD-11 mapping available for E74.810 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.