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 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)
- dietary mineral deficiency (E58-E61)
- parathyroid disorders (E20-E21)
- vitamin D deficiency (E55.-)
- iron deficiency anemia (D50.-)
- sideroblastic anemia (D64.0-D64.3)
- GALD (P78.84)
- Gestational alloimmune liver disease (P78.84)
- Neonatal hemochromatosis (P78.84)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
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
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.
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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.