E83.119
BillableHemochromatosis, unspecified
Hemochromatosis, unspecified
Coding Notes
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
- •dietary mineral deficiencyE58-E61
- •parathyroid disordersE20-E21
- •vitamin D deficiencyE55
- •iron deficiency anemiaD50
- •sideroblastic anemiaD64.0-D64.3
- •GALDP78.84
- •Gestational alloimmune liver diseaseP78.84
- •Neonatal hemochromatosisP78.84
Related Codes(3)
Also Known As / Clinical Terms(131)
SNOMED CT
- Dilated cardiomyopathy due to haemochromatosis8209004
- Dilated cardiomyopathy due to hemochromatosis8209004
- Dilated cardiomyopathy secondary to haemochromatosis8209004
- Dilated cardiomyopathy secondary to hemochromatosis8209004
- Restrictive cardiomyopathy secondary to haemochromatosis56941009
- Restrictive cardiomyopathy secondary to hemochromatosis56941009
- Dilated cardiomyopathy due to infiltration64749001
- Infiltrative dilated cardiomyopathy64749001
- Dilated cardiomyopathy due to metabolic disorder111285003
- Dilated cardiomyopathy secondary to metabolic disorder111285003
- Metabolic cardiomyopathy111285003
- Latent haemochromatosis343570008
- Latent hemochromatosis343570008
- Haemochromatosis399187006
- Hemochromatosis399187006
- Iron storage disease399187006
- Secondary restrictive cardiomyopathy415509000
- Hypoparathyroidism due to haemochromatosis717901001
- Hypoparathyroidism due to hemochromatosis717901001
- Infiltrative cardiomyopathy871646007
UMLS
- Bronze DiabetesC0018995
- Bronze diabetesC0018995
- Bronze diabetes (disorder)C0018995
- Bronzed CirrhosesC0018995
- Bronzed CirrhosisC0018995
- Bronzed diabetesC0018995
- Cirrhoses, BronzedC0018995
- Cirrhoses, PigmentaryC0018995
- Cirrhosis, BronzedC0018995
- Cirrhosis, PigmentaryC0018995
- Diabetes, BronzeC0018995
- Disease, Von Recklenhausen-ApplebaumC0018995
- Diseases, Von Recklenhausen-ApplebaumC0018995
- Disorder, Iron StorageC0018995
- Disorders, Iron StorageC0018995
- HaemochromatosesC0018995
- HaemochromatosisC0018995
- HemochromatoseC0018995
- HemochromatosesC0018995
- HemochromatosisC0018995
- Hemochromatosis (disorder)C0018995
- Hemochromatosis, unspecifiedC0018995
- HemosiderosisC0018995
- Iron Overload DiseaseC0018995
- Iron Storage DisorderC0018995
- Iron Storage DisordersC0018995
- Iron overload diseaseC0018995
- Iron storage diseaseC0018995
- Iron storage disorderC0018995
- Pigmentary CirrhosesC0018995
- Pigmentary CirrhosisC0018995
- Recklenhausen-Applebaum Disease, VonC0018995
- Recklenhausen-Applebaum Diseases, VonC0018995
- Storage Disorder, IronC0018995
- Storage Disorders, IronC0018995
- Syndrome, Troisier-Hanot-ChauffardC0018995
- Syndromes, Troisier-Hanot-ChauffardC0018995
- Troisier Hanot Chauffard SyndromeC0018995
- Troisier-Hanot-Chauffard SyndromeC0018995
- Troisier-Hanot-Chauffard SyndromesC0018995
- Troisier-Hanot-Chauffard syndromeC0018995
- Von Recklenhausen Applebaum DiseaseC0018995
- Von Recklenhausen-Applebaum DiseaseC0018995
- Von Recklenhausen-Applebaum DiseasesC0018995
- Von Recklenhausen-Applebaum diseaseC0018995
- bronze diabetesC0018995
- bronzed diabetesC0018995
- diabetes bronzeC0018995
- disorders iron storageC0018995
- haemochromatosisC0018995
- hemochromatosesC0018995
- hemochromatosisC0018995
- iron storage diseaseC0018995
- iron storage disorderC0018995
Clinical Terms
- Secondary restrictive cardiomyopathy
- iron storage disorder
- Dilated cardiomyopathy due to metabolic disorder
- Diabetes, Bronze
- Iron Storage Disorders
- Hypoparathyroidism due to hemochromatosis
- Bronze diabetes (disorder)
- Bronze diabetes
- Syndrome, Troisier-Hanot-Chauffard
- Storage Disorder, Iron
- Pigmentary Cirrhoses
- Troisier-Hanot-Chauffard syndrome
- Hemochromatosis (disorder)
- Latent haemochromatosis
- Disorder, Iron Storage
- Disease, Von Recklenhausen-Applebaum
- Bronzed diabetes
- diabetes bronze
- Dilated cardiomyopathy due to haemochromatosis
- Cirrhosis, Pigmentary
- Disorders, Iron Storage
- Von Recklenhausen-Applebaum disease
- Iron Overload Disease
- Pigmentary Cirrhosis
- Cirrhosis, Bronzed
- Dilated cardiomyopathy secondary to hemochromatosis
- Dilated cardiomyopathy secondary to metabolic disorder
- Latent hemochromatosis
- Bronzed Cirrhoses
- Hemosiderosis
- Cirrhoses, Bronzed
- Diseases, Von Recklenhausen-Applebaum
- Recklenhausen-Applebaum Disease, Von
- Iron storage disease
- Metabolic cardiomyopathy
- Bronzed Cirrhosis
- Storage Disorders, Iron
- Restrictive cardiomyopathy secondary to haemochromatosis
- disorders iron storage
- Hemochromatoses
- Von Recklenhausen Applebaum Disease
- Dilated cardiomyopathy due to hemochromatosis
- Infiltrative dilated cardiomyopathy
- Hypoparathyroidism due to haemochromatosis
- Dilated cardiomyopathy secondary to haemochromatosis
- Recklenhausen-Applebaum Diseases, Von
- Infiltrative cardiomyopathy
- Restrictive cardiomyopathy secondary to hemochromatosis
- Hemochromatose
- haemochromatosis
- Haemochromatoses
- Cirrhoses, Pigmentary
- Troisier-Hanot-Chauffard Syndromes
- Troisier Hanot Chauffard Syndrome
- Von Recklenhausen-Applebaum Diseases
- Syndromes, Troisier-Hanot-Chauffard
- Dilated cardiomyopathy due to infiltration
Frequently Asked Questions
What is the ICD-10 code for hemochromatosis, unspecified?
The ICD-10-CM code for hemochromatosis, unspecified is E83.119. The full clinical description is "Hemochromatosis, unspecified". E83.119 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E83.119 mean?
ICD-10-CM code E83.119 represents “Hemochromatosis, unspecified”. 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 E83.119 a billable code?
Yes, E83.119 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E83.119 in?
E83.119 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E83.119?
E83.119 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 11 more.
What SNOMED CT codes does E83.119 map to?
E83.119 maps to 9 SNOMED CT concepts: 8209004, 64749001, 111285003, 399187006, 717901001, and 4 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E83.119?
E83.119 is linked to 1 UMLS Concept Unique Identifier: C0018995. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E83.119 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hemochromatosis, unspecified 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 E83.119?
There is no direct ICD-11 mapping available for E83.119 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.