E72.02
BillableHartnup's disease
Hartnup's disease
Coding Notes
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)
- disorders of:
- aromatic amino-acid metabolism (E70.-)
- branched-chain amino-acid metabolism (E71.0-E71.2)
- fatty-acid metabolism (E71.3)
- purine and pyrimidine metabolism (E79.-)
- gout (M1A.-, M10.-)
- disorders of tryptophan metabolism (E70.5)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Hartnup disorder, renal type22011005
- Hartnup disorder, renal/jejunal type36891003
- Hartnup disease80902009
- Hartnup disorder80902009
- Neutral 1 amino acid transport defect80902009
- Neutral amino acid transport defect80902009
- Dystonia due to Hartnup disease1260399002
- Dystonia due to neutral 1 amino acid transport defect1260399002
UMLS
- AA TRANSPORT DIS NEUTRALC0018609
- Amino Acid Transport Disorder, NeutralC0018609
- HARTNUP DISC0018609
- HARTNUP DISEASEC0018609
- HARTNUP DISORDERC0018609
- HNDC0018609
- Hartnup DiseaseC0018609
- Hartnup DisorderC0018609
- Hartnup diseaseC0018609
- Hartnup disorderC0018609
- Hartnup's diseaseC0018609
- NEUTRAL AA TRANSPORT DEFECTC0018609
- NEUTRAL AA TRANSPORT DISC0018609
- Neutral 1 amino acid transport defectC0018609
- Neutral 1 amino acid transport defect (disorder)C0018609
- Neutral Amino Acid Transport DefectC0018609
- Neutral Amino Acid Transport DisorderC0018609
- Neutral amino acid transport defectC0018609
- TRANSPORT DIS NEUTRAL AAC0018609
- TRANSPORT DIS NEUTRAL AMINO ACIDSC0018609
- Transport Disorder, Neutral Amino AcidC0018609
- Transport Disorder, Neutral Amino AcidsC0018609
- disease hartnupC0018609
- disease hartnupsC0018609
- h diseaseC0018609
- hart syndromeC0018609
- hartnup diseaseC0018609
- hartnup disorderC0018609
- neutral amino acid transport defectC0018609
Frequently Asked Questions
What is the ICD-10 code for hartnup's disease?
The ICD-10-CM code for hartnup's disease is E72.02. The full clinical description is "Hartnup's disease". E72.02 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E72.02 mean?
ICD-10-CM code E72.02 represents "Hartnup's 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 E72.02 a billable code?
Yes, E72.02 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E72.02 in?
E72.02 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E72.02?
E72.02 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 10 more.
What SNOMED CT codes does E72.02 map to?
E72.02 maps to 4 SNOMED CT concepts: 1260399002, 80902009, 22011005, 36891003. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E72.02?
E72.02 is linked to 1 UMLS Concept Unique Identifier: C0018609. 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.