E83.110
BillableHereditary hemochromatosis
E83.110 is the ICD-10-CM code for Hereditary hemochromatosis. It is a billable, specific code valid for reimbursement.
E00-E89 Endocrine, nutritional and metabolic diseases
What this means — in plain language
MedlinePlus · NIHHemochromatosis is a disease in which too much iron builds up in your body. Your body needs iron but too much of it is toxic. If you have hemochromatosis, you absorb more iron than you need. Your body has no natural way to get rid of the extra iron. It stores it in body tissues, especially the liver, heart, and pancreas. The extra iron can damage your organs. Without treatment, it can cause your organs to fail.…
Read more about Hemochromatosis at MedlinePlus ↗Source: U.S. National Library of Medicine (MedlinePlus). Informational only — not medical advice.
Includes
- •Bronzed diabetes
- •Pigmentary cirrhosis (of liver)
- •Primary (hereditary) hemochromatosis
Medications indicated for this condition
FDA labeling- CalcitriolVitamin D3 Analog [EPC]›
- Calcium Chloride›
- Calcium Gluconate›
- Cinacalcet›
- ErgocalciferolProvitamin D2 Compound [EPC]›
- Magnesium Sulfate›
- Magnesium Sulfate Heptahydrate›
- PenicillamineAntirheumatic Agent [EPC]›
- Potassium Phosphate›
- Salmon CalcitoninCalcitonin [EPC]›
- Marcaine, Lidocaine, Kenalog, Povidone Iodine›
- Trientine›
Drugs whose FDA labeling lists this condition's category among its indications. Informational only — not a treatment recommendation or medical advice.
Conditions mapped to this code
MedlinePlus · NIHPlain-language health-topic references grounded in MedlinePlus (NIH/NLM).
Frequently asked questions
Source: CMS ICD-10-CM FY2026. For informational purposes only — not medical advice. See our medical disclaimer.
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