E80.5
BillableCrigler-Najjar syndrome
Crigler-Najjar 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
- Bilirubin UDP glucuronyl transferase deficiency8933000
- Bilirubin glucuronosyltransferase deficiency8933000
- Crigler-Najjar syndrome type I8933000
- Crigler-Najjar syndrome, type I8933000
- Crigler-Najjar type 18933000
- Deficiency of glucuronosyltransferase8933000
- Glucuronyltransferase deficiency8933000
- UDP glucuronyl transferase deficiency8933000
- Crigler-Najjar syndrome28259009
- Arias syndrome68067009
- Crigler-Najjar syndrome type II68067009
- Crigler-Najjar syndrome, type II68067009
- Crigler-Najjar type 268067009
- Neonatal jaundice due to Crigler-Najjar syndrome206454000
UMLS
- CRIGLER-NAJJAR SYNDROMEC5551003
- Crigler Najar SyndromeC5551003
- Crigler Najjar SyndromeC5551003
- Crigler Najjar SyndromesC5551003
- Crigler Najjar syndromeC5551003
- Crigler-Najar SyndromeC5551003
- Crigler-Najjar SyndromeC5551003
- Crigler-Najjar syndromeC5551003
- Crigler-Najjar syndrome (disorder)C5551003
- Familial Nonhemolytic Unconjugated HyperbilirubinemiaC5551003
- Familial nonhemolytic unconjugated hyperbilirubinemiaC5551003
- Hereditary Unconjugated HyperbilirubinemiaC5551003
- Hereditary Unconjugated HyperbilirubinemiasC5551003
- Hereditary unconjugated hyperbilirubinemiaC5551003
- Hyperbilirubinemia, Hereditary UnconjugatedC5551003
- Najjar Syndrome, CriglerC5551003
- Syndrome, Crigler NajjarC5551003
- Unconjugated Hyperbilirubinemia, HereditaryC5551003
- crigler najjar syndromeC5551003
- crigler najjar syndromesC5551003
- crigler-najjar diseaseC5551003
- crigler-najjar syndromeC5551003
Frequently Asked Questions
What is the ICD-10 code for crigler-najjar syndrome?
The ICD-10-CM code for crigler-najjar syndrome is E80.5. The full clinical description is "Crigler-Najjar syndrome". E80.5 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E80.5 mean?
ICD-10-CM code E80.5 represents "Crigler-Najjar syndrome". 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 E80.5 a billable code?
Yes, E80.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E80.5 in?
E80.5 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E80.5?
E80.5 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 E80.5 map to?
E80.5 maps to 5 SNOMED CT concepts: 68067009, 8933000, 28259009, 5655007, 206454000. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E80.5?
E80.5 is linked to 1 UMLS Concept Unique Identifier: C5551003. 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.