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 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
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
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.
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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.