E83.19

Billable

Other disorders of iron metabolism

Other disorders of iron metabolism

Status

Billable / Specific

Block

E70-E88

Parent Code

E83.1

Coding Notes

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

Use Additional Code

Additional codes that should follow this code

Related Codes(2)
E83.10

Disorder of iron metabolism, unspecified

BillableE83.11

Hemochromatosis

Also Known As / Clinical Terms(129)

SNOMED CT

UMLS

Clinical Terms

  • IPH - Idiopathic pulmonary haemosiderosis
  • Transfusion induced iron overload
  • Neurodegeneration with brain iron accumulation due to COASY mutation
  • Skin pigmentation due to haemosiderosis
  • Coenzyme A synthase protein associated neurodegeneration
  • Haemosiderosis, acquired
  • Pulmonary haemosiderosis
  • Shunt hemosiderosis
  • Haemosiderosis
  • Haemosiderin pigmentation of skin due to venous insufficiency
  • Lower limb hemosiderosis due to venous insufficiency
  • Idiopathic pulmonary haemosiderosis
  • L-ferritin deficiency
  • Hemosiderosis, acquired
  • Skin pigmentation due to hemosiderosis
  • Endogenous non-melanin pigmentation
  • Brown induration of lung
  • Secondary hemosiderosis
  • Transfusion haemosiderosis
  • Static encephalopathy of childhood with neurodegeneration in adulthood
  • Secondary haemosiderosis
  • Hemosiderosis, primary
  • Low serum ferritin
  • Serum ferritin level low
  • Cutaneous hemosiderosis
  • Hemosiderosis of lower limb due to venous insufficiency
  • CoPAN - coenzyme A synthase protein associated neurodegeneration
  • Beta-propeller protein-associated neurodegeneration
  • Deficiency of ferroxidase
  • Deficiency of caeruloplasmin
  • IPH - Idiopathic pulmonary hemosiderosis
  • Pulmonary hemosiderosis
  • Secondary pulmonary haemosiderosis
  • Hemosiderosis
  • Cerebro-cutaneous syndrome with iron overload
  • Neurodegeneration with brain iron accumulation type 5
  • Renal hemosiderosis
  • Haemosiderosis, primary
  • Deficiency of ceruloplasmin
  • Ferro-cerebro-cutaneous syndrome
  • BPAN - beta-propeller protein-associated neurodegeneration
  • Ferritin level low
  • Haemosiderosis of lower limb due to venous insufficiency
  • Hepatic haemosiderosis
  • Hemosiderin pigmentation of skin due to venous insufficiency
  • Focal haemosiderosis
  • Neonatal iron overload
  • Iron overload
  • Shunt haemosiderosis
  • Focal hemosiderosis
  • Idiopathic pulmonary hemosiderosis
  • Renal haemosiderosis
  • Serum ferritin level below reference range
  • Secondary pulmonary hemosiderosis
  • COASY protein-associated neurodegeneration
  • Cutaneous haemosiderosis
  • Lower limb haemosiderosis due to venous insufficiency
  • Venous pigmentation of skin
  • Iron excess
  • LFTD - L-ferritin deficiency
  • Increased storage iron
  • Transfusion hemosiderosis
  • Hepatic hemosiderosis
  • Ferritin level below reference range
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, also report: 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.

How does E83.19 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders of iron metabolism 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 E83.19?

There is no direct ICD-11 mapping available for E83.19 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.