E83.111 is the authoritative medical code for Hemochromatosis due to repeated red blood cell transfusions. This classification is used in medical billing and clinical recording to specify the clinical criteria for hemochromatosis due to repeated red blood cell transfusions (ICD-10-CM E83.111), ensuring healthcare documentation aligns with 2026 federal coding standards.
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Official Registry Overview & Definition
Hemochromatosis due to repeated red blood cell transfusions is a billable ICD-10-CM diagnosis code E83.111. Inclusion terms: Iron overload due to repeated red blood cell transfusions; Transfusion (red blood cell) associated hemochromatosis. Excludes1 (not coded here): GALD P78.84; Gestational alloimmune liver disease P78.84; Neonatal hemochromatosis P78.84; iron deficiency anemia D50.-; sideroblastic anemia D64.0-D64.3; dietary mineral deficiency E58-E61; parathyroid disorders E20-E21; vitamin D deficiency E55.-; 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. Excludes2 (not included here): Ehlers-Danlos syndromes Q79.6-.
Official Tabular Instructional Notes
Sequencing, inclusion, and exclusion notes published for E83.111 in the official ICD-10-CM tabular list.
Inclusion Terms
Alternative terms the tabular list files under this code.
- Iron overload due to repeated red blood cell transfusions
- Transfusion (red blood cell) associated hemochromatosis
Excludes1 — Not Coded Here
Conditions that can never be reported with this code; the two are mutually exclusive.
- GALD P78.84
- Gestational alloimmune liver disease P78.84
- Neonatal hemochromatosis P78.84
- iron deficiency anemia D50.-
- sideroblastic anemia D64.0-D64.3
- dietary mineral deficiency E58-E61
- parathyroid disorders E20-E21
- vitamin D deficiency E55.-
- 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
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- Ehlers-Danlos syndromes Q79.6-
Frequently Asked Questions (FAQ) & Clinical Guidance
What can't be coded together with E83.111?
Per Excludes1 instructions, E83.111 must not be reported with: GALD (P78.84); Gestational alloimmune liver disease (P78.84); Neonatal hemochromatosis (P78.84); iron deficiency anemia (D50.-).
Can E83.111 be reported alongside related conditions?
Per Excludes2 instructions, E83.111 and the following may both be reported when both are present: Ehlers-Danlos syndromes (Q79.6-).
What conditions are included under E83.111?
Hemochromatosis due to repeated red blood cell transfusions includes: Iron overload due to repeated red blood cell transfusions; Transfusion (red blood cell) associated hemochromatosis.
Codes in This Family (39)
Official ICD-10-CM classifications in the same code family as E83.111, with their registry titles.
- E83 — Disorders of mineral metabolism
- E83.0 — Disorders of copper metabolism
- E83.00 — Disorder of copper metabolism, unspecified
- E83.01 — Wilson's disease
- E83.09 — Other disorders of copper metabolism
- E83.1 — Disorders of iron metabolism
- E83.10 — Disorder of iron metabolism, unspecified
- E83.11 — Hemochromatosis
- E83.110 — Hereditary hemochromatosis
- E83.118 — Other hemochromatosis
- E83.119 — Hemochromatosis, unspecified
- E83.19 — Other disorders of iron metabolism
- E83.2 — Disorders of zinc metabolism
- E83.3 — Disorders of phosphorus metabolism and phosphatases
- E83.30 — Disorder of phosphorus metabolism, unspecified
- E83.31 — Familial hypophosphatemia
- E83.32 — Hereditary vitamin D-dependent rickets (type 1) (type 2)
- E83.39 — Other disorders of phosphorus metabolism
- E83.4 — Disorders of magnesium metabolism
- E83.40 — Disorders of magnesium metabolism, unspecified
- E83.41 — Hypermagnesemia
- E83.42 — Hypomagnesemia
- E83.49 — Other disorders of magnesium metabolism
- E83.5 — Disorders of calcium metabolism
- E83.50 — Unspecified disorder of calcium metabolism
- E83.51 — Hypocalcemia
- E83.52 — Hypercalcemia
- E83.59 — Other disorders of calcium metabolism
- E83.8 — Other disorders of mineral metabolism
- E83.81 — Hungry bone syndrome
- E83.82 — Disorders of pyrophosphate metabolism
- E83.820 — Generalized arterial calcification of infancy with unspecified genetic causality
- E83.821 — ENPP1 deficiency causing generalized arterial calcification of infancy
- E83.822 — ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
- E83.823 — ABCC6 deficiency causing generalized arterial calcification of infancy
- E83.824 — ABCC6 deficiency causing pseudoxanthoma elasticum
- E83.825 — CD73 deficiency causing arterial calcification
- E83.89 — Other disorders of mineral metabolism
- E83.9 — Disorder of mineral metabolism, unspecified
Indexed Clinical Terms (4)
Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code.
- Complication (s) (from) (of), transfusion (blood) (lymphocytes) (plasma), hemochromatosis
- Hemochromatosis, due to repeated red blood cell transfusion
- Overload, iron, due to repeated red blood cell transfusions
- Transfusion, associatedhemochromatosis (red blood cell)
Related Codes & Numerical Sequence (Crawl Map)
Search engines and indexers are advised to traverse adjacent medical codes in this sub-chapter range to find correlated diagnoses or therapeutic procedures: