E80.4
BillableGilbert syndrome
Gilbert syndrome
Coding Notes
Includes
Conditions included under this code
- defects of catalase and peroxidase
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Inherited disorder of bilirubin metabolism5655007
- Benign unconjugated bilirubinaemia syndrome27503000
- Benign unconjugated bilirubinemia syndrome27503000
- Cholaemia familiaris simplex27503000
- Cholemia familiaris simplex27503000
- Chronic intermittent juvenile jaundice27503000
- Congenital familial cholaemia27503000
- Congenital familial cholemia27503000
- Constitutional hepatic dysfunction27503000
- Familial nonhaemolytic bilirubinaemia27503000
- Familial nonhaemolytic jaundice27503000
- Familial nonhemolytic bilirubinemia27503000
- Familial nonhemolytic jaundice27503000
- Gilbert syndrome27503000
- Gilbert's disease27503000
- Gilbert's syndrome27503000
- Gilbert-Lereboullet syndrome27503000
- Gilberts syndrome27503000
- Hereditary nonhaemolytic jaundice27503000
- Hereditary nonhemolytic jaundice27503000
- Low-grade chronic hyperbilirubinaemia syndrome27503000
- Low-grade chronic hyperbilirubinemia syndrome27503000
- Meulengracht syndrome27503000
- Neonatal jaundice due to Gilbert syndrome206456003
- Neonatal jaundice due to Gilbert's syndrome206456003
UMLS
- Arias Type HyperbilirubinemiaC0017551
- Arias Type HyperbilirubinemiasC0017551
- Benign unconjugated bilirubinaemia syndromeC0017551
- Benign unconjugated bilirubinemia syndromeC0017551
- Cholaemia familiaris simplexC0017551
- Cholemia familiaris simplexC0017551
- Chronic intermittent juvenile jaundiceC0017551
- Congenital familial cholaemiaC0017551
- Congenital familial cholemiaC0017551
- Constitutional Liver DysfunctionC0017551
- Constitutional hepatic dysfunctionC0017551
- Constitutional liver dysfunctionC0017551
- Disease, GilbertC0017551
- Disease, Gilbert'sC0017551
- Familial Nonhemolytic JaundiceC0017551
- Familial nonhaemolytic bilirubinaemiaC0017551
- Familial nonhaemolytic jaundiceC0017551
- Familial nonhemolytic bilirubinemiaC0017551
- Familial nonhemolytic jaundiceC0017551
- GILBERT DISC0017551
- GILBERT SYNDROMEC0017551
- GILBERTS DISC0017551
- Gilbert DiseaseC0017551
- Gilbert SyndromeC0017551
- Gilbert diseaseC0017551
- Gilbert syndromeC0017551
- Gilbert's DiseaseC0017551
- Gilbert's SyndromeC0017551
- Gilbert's diseaseC0017551
- Gilbert's syndromeC0017551
- Gilbert's syndrome (disorder)C0017551
- Gilbert-Lereboullet SyndromeC0017551
- Gilbert-Lereboullet syndromeC0017551
- Gilberts DiseaseC0017551
- Gilberts SyndromeC0017551
- Gilberts syndromeC0017551
- HBLRGC0017551
- HYPERBILIRUBINEMIA IC0017551
- HYPERBILIRUBINEMIA, ARIAS TYPEC0017551
- HYPERBILIRUBINEMIA, GILBERT TYPEC0017551
- Hereditary nonhaemolytic jaundiceC0017551
- Hereditary nonhemolytic jaundiceC0017551
- Hyperbilirubinemia 1C0017551
- Hyperbilirubinemia 1sC0017551
- Hyperbilirubinemia IC0017551
- Hyperbilirubinemia, Arias TypeC0017551
- Hyperbilirubinemias, Arias TypeC0017551
- Jaundice, congenital nonhemolyticC0017551
- Low-grade chronic hyperbilirubinaemia syndromeC0017551
- Low-grade chronic hyperbilirubinemia syndromeC0017551
- Meulengracht SyndromeC0017551
- Meulengracht syndromeC0017551
- Syndrome, GilbertC0017551
- Syndrome, Gilbert'sC0017551
- Unconjugated Benign BilirubinemiaC0017551
- Unconjugated benign bilirubinemiaC0017551
- congenital nonhemolytic jaundiceC0017551
- diseases gilbertC0017551
- familial nonhemolytic jaundiceC0017551
- gilbert diseaseC0017551
- gilbert syndromeC0017551
- gilbert syndromesC0017551
- gilbert's diseaseC0017551
- gilbert's syndromeC0017551
- gilberts diseaseC0017551
- gilberts syndromeC0017551
- hereditary nonhemolytic jaundiceC0017551
- meulengracht syndromeC0017551
- syndrome gilbert'sC0017551
Frequently Asked Questions
What is ICD-10 code E80.4?
ICD-10-CM code E80.4 represents "Gilbert syndrome". It is a billable/specific code that can be used on a claim.
Is E80.4 a billable code?
Yes, E80.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E80.4 in?
E80.4 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E80.4?
E80.4 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 3 more.
What SNOMED CT codes does E80.4 map to?
E80.4 maps to 3 SNOMED CT concepts: 27503000, 5655007, 206456003. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E80.4?
E80.4 is linked to 1 UMLS Concept Unique Identifier: C0017551. 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.