E83.19
BillableOther disorders of iron metabolism
Other disorders of iron metabolism
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)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Use Additional Code
Additional codes that should follow this code
- code, if applicable, for idiopathic pulmonary hemosiderosis (J84.03)
Also Known As / Clinical Terms
SNOMED CT
- Focal haemosiderosis10180006
- Focal hemosiderosis10180006
- Haemosiderosis39011001
- Hemosiderosis39011001
- Secondary haemosiderosis39784009
- Secondary hemosiderosis39784009
- Brown induration of lung40527005
- IPH - Idiopathic pulmonary haemosiderosis40527005
- IPH - Idiopathic pulmonary hemosiderosis40527005
- Idiopathic pulmonary haemosiderosis40527005
- Idiopathic pulmonary hemosiderosis40527005
- Pulmonary haemosiderosis40527005
- Pulmonary hemosiderosis40527005
- Increased storage iron60737008
- Iron excess60737008
- Iron overload60737008
- Transfusion haemosiderosis69281008
- Transfusion hemosiderosis69281008
- Transfusion induced iron overload69281008
- Shunt haemosiderosis72825009
- Shunt hemosiderosis72825009
- Renal haemosiderosis83563007
- Renal hemosiderosis83563007
- Hepatic haemosiderosis83761007
- Hepatic hemosiderosis83761007
- Deficiency of caeruloplasmin124224004
- Deficiency of ceruloplasmin124224004
- Deficiency of ferroxidase124224004
- Ferritin level below reference range165626000
- Ferritin level low165626000
- Haemosiderosis, primary190846002
- Hemosiderosis, primary190846002
- Haemosiderosis, acquired190847006
- Hemosiderosis, acquired190847006
- Endogenous non-melanin pigmentation402618006
- Cutaneous haemosiderosis403261006
- Cutaneous hemosiderosis403261006
- Skin pigmentation due to haemosiderosis403261006
- Skin pigmentation due to hemosiderosis403261006
- Haemosiderin pigmentation of skin due to venous insufficiency403262004
- Hemosiderin pigmentation of skin due to venous insufficiency403262004
- Venous pigmentation of skin403262004
- Haemosiderosis of lower limb due to venous insufficiency703280000
- Hemosiderosis of lower limb due to venous insufficiency703280000
- Lower limb haemosiderosis due to venous insufficiency703280000
- Lower limb hemosiderosis due to venous insufficiency703280000
- Secondary pulmonary haemosiderosis716712004
- Secondary pulmonary hemosiderosis716712004
- COASY protein-associated neurodegeneration732264002
- CoPAN - coenzyme A synthase protein associated neurodegeneration732264002
- Coenzyme A synthase protein associated neurodegeneration732264002
- Neurodegeneration with brain iron accumulation due to COASY mutation732264002
- BPAN - beta-propeller protein-associated neurodegeneration732959007
- Beta-propeller protein-associated neurodegeneration732959007
- Neurodegeneration with brain iron accumulation type 5732959007
- Static encephalopathy of childhood with neurodegeneration in adulthood732959007
- Cerebro-cutaneous syndrome with iron overload774151000
- Ferro-cerebro-cutaneous syndrome774151000
- Neonatal iron overload1142071000
- L-ferritin deficiency1217208003
- LFTD - L-ferritin deficiency1217208003
- Low serum ferritin126121000119104
- Serum ferritin level below reference range126121000119104
- Serum ferritin level low126121000119104
Frequently Asked Questions
What is the ICD-10 code for other disorders of iron metabolism?
The ICD-10-CM code for other disorders of iron metabolism is E83.19. The full clinical description is "Other disorders of iron metabolism". E83.19 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E83.19 mean?
ICD-10-CM code E83.19 represents "Other disorders of iron metabolism". 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 E83.19 a billable code?
Yes, E83.19 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E83.19 in?
E83.19 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E83.19?
E83.19 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 8 more.
Are additional codes required with E83.19?
Yes, when using E83.19 you should also code: code, if applicable, for idiopathic pulmonary hemosiderosis (J84.03).
What SNOMED CT codes does E83.19 map to?
E83.19 maps to 24 SNOMED CT concepts: 732959007, 40527005, 732264002, 774151000, 403261006, and 19 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E83.19?
E83.19 is linked to 1 UMLS Concept Unique Identifier: C2874299. 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.