E83.11 ICD-10-CM Code: Hemochromatosis
Billing Status: NO. This is a clinician non-billable / parent hierarchy grouping in the ICD-10-CM system.
Coding at a Glance
- Tabular directives
- 13 Excludes1 · 1 Excludes2
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for E83.11 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2026Effective: October 1, 2025
Notes without a marker are published on E83.11 itself; “inherited from” names the category or block whose note applies here.
Excludes1 — Not Coded Here
Conditions generally not reported together with this code (Excludes1) -- an error unless the two conditions are documented as unrelated to each other (ICD-10-CM Official Guidelines, Section I.A.12.a).
- GALD (P78.84) Compare E83.11 vs P78.84 →
- Gestational alloimmune liver disease (P78.84) Compare E83.11 vs P78.84 →
- Neonatal hemochromatosis (P78.84) Compare E83.11 vs P78.84 →
- iron deficiency anemia (D50.-) inherited from E83.1Compare E83.11 vs D50 →
- sideroblastic anemia (D64.0-D64.3) inherited from E83.1Compare E83.11 vs D64.0 →
- dietary mineral deficiency (E58-E61) inherited from E83Compare E83.11 vs E58 →
- parathyroid disorders (E20-E21) inherited from E83Compare E83.11 vs E20 →
- vitamin D deficiency (E55.-) inherited from E83Compare E83.11 vs E55 →
- androgen insensitivity syndrome (E34.5-) inherited from E70-E88Compare E83.11 vs E34.5 →
- congenital adrenal hyperplasia (E25.0) inherited from E70-E88Compare E83.11 vs E25.0 →
- hemolytic anemias attributable to enzyme disorders (D55.-) inherited from E70-E88Compare E83.11 vs D55 →
- Marfan syndrome (Q87.4-) inherited from E70-E88Compare E83.11 vs Q87.4 →
- 5-alpha-reductase deficiency (E29.1) inherited from E70-E88Compare E83.11 vs 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-) Compare E83.11 vs Q79.6 →
Source: inherited from E70-E88
Coder workflow for E83.11
MedCoder structured workflow — derived from this code’s own official record
Before you code E83.11
- E83.11 is not reportable as written. Select the more specific code beneath it that the documentation supports. Codes are reported to the highest level of specificity the classification provides (Guidelines I.B.2).
ReviewE83.110, E83.111, E83.118, E83.119
See the relationships section · Guide: How to choose an ICD-10-CM code →
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with E83.11. Excludes1 conditions are not reported together with this code unless the record shows they are unrelated (Guidelines I.A.12.a).
Choose the right path
- Does the documentation support one of the more specific codes beneath E83.11?
Yes → Select that code and continue the checks below on its own page.
No → E83.11 cannot be reported as written; query for the specificity its subcategory needs. - Does the documentation support a condition named in E83.11’s Excludes1 note?
Yes → Do not simply proceed: review the excluded code. Both are reported only when the record shows the two conditions are unrelated.
No → Continue.
Consider E83.11. Then confirm the code is valid for the date of service in the Verify section.
Documentation check
- The provider’s diagnostic statement
- Codes are assigned from the provider’s documented diagnosis, not from clinical criteria, test values or a medication list (Guidelines I.A.19).
Official instructions as workflow
Excludes1 — check before selecting E83.11(13 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with E83.11: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
CompareP78.84, D50, E55, E34.5, E25.0, D55
See the official tabular notes · Guidelines I.A.12.a
Excludes2 — not part of E83.11(1 note)
Coding workflow: The conditions named in this note are not included in E83.11. When the record documents both, both may be reported; the note is a boundary, not a prohibition.
CompareQ79.6
See the official tabular notes · Guidelines I.A.12.b
Coding decision scenarios
Pattern scenarios for this code’s structure — decision rules, not clinical cases
Documentation: Both the condition E83.11 describes and a condition named in its Excludes1 note are documented for the same encounter.
Coding question: Can both codes be reported?
Path: Review the Excludes1 note and the excluded code, and look for a provider statement on whether the two conditions are related.
Reason: Excludes1 means the two are not coded together; the exception is when the record shows the conditions are unrelated to each other (Guidelines I.A.12.a).
Every row is derived from this code’s own record — its title, tabular notes, 7th-character family and same-category siblings — with fixed MedCoder wording; nothing is inferred about a patient. The official notes and guideline text are in the sections each row links to, and they control.
Code Overview
MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.
Verify Before Coding
From the code registry, the Medicare Code Editor, and the MS-DRG Definitions Manual. Check it against a full claim in Claim Check.
Relationships & Classification
MedCoder structured relationships — computed from published CMS and AHRQ datasets
Other codes that name E83.11 or its code family, from the CMS ICD-10-CM tabular instructional notes. Tabular-note edges are stored at the code family level that carries each note.
Referenced by 4 Excludes1 notes across 3 chapters: E61 — Deficiency of other nutrient elements (via E83.-), P59 — Neonatal jaundice from other and unspecified causes (via E83.-), P78.84 — Gestational alloimmune liver disease, R79.0 — Abnormal level of blood mineral (via E83.-).
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Referenced by 13 Excludes2 notes across 3 chapters: G11 — Hereditary ataxia (via E83.-), G71 — Primary disorders of muscles (via E83.-), K70 — Alcoholic liver disease, K70-K77 — Diseases of liver (K70-K77), K71 — Toxic liver disease, K72 — Hepatic failure, not elsewhere classified, K73 — Chronic hepatitis, not elsewhere classified, K74 — Fibrosis and cirrhosis of liver, K75 — Other inflammatory liver diseases, K76 — Other diseases of liver, K77 — Liver disorders in diseases classified elsewhere, N25.0 — Renal osteodystrophy (via E83.-), N25.81 — Secondary hyperparathyroidism of renal origin (via E83.-).
These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.
Referenced by 4 Code First instructions across 4 chapters: G63 — Polyneuropathy in diseases classified elsewhere (via E83.-), H42 — Glaucoma in diseases classified elsewhere (via E83.-), J84.03 — Idiopathic pulmonary hemosiderosis (via E83.1.-), M14.8 — Arthropathies in other specified diseases classified elsewhere.
Each of these codes carries a Code First note naming this condition — when that code is reported, THIS code is sequenced first, ahead of it.
Related Codes
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main term “Hemosiderosis”; these codes share that main term but sit in a different category of the Tabular List.
T80.89 — Other complications following infusion, transfusion and therapeutic injection
Contextual Map
Every relationship of E83.11 in one view: hierarchy, official tabular instructions in both directions, clinical classification, risk adjustment, MS-DRG participation, index terms and change history — each edge carrying the CMS source it derives from.
Run E83.11 with these 16 related codes in Claim Check
Hierarchy
- E00-E89 — Chapter 4: Endocrine, Nutritional and Metabolic Diseases (E00-E89) (E00-E89)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E70-E88 — Metabolic disorders[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Excludes1
- P78.84 — Gestational alloimmune liver disease[Excludes1]: “GALD (P78.84)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Excludes1 notes
- E61 — Deficiency of other nutrient elements[Excludes1](via E83.-): “disorders of mineral metabolism (E83.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- P59 — Neonatal jaundice from other and unspecified causes[Excludes1](via E83.-): “jaundice due to inborn errors of metabolism (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- P78.84 — Gestational alloimmune liver disease[Excludes1]: “hemochromatosis (E83.11-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- R79.0 — Abnormal level of blood mineral[Excludes1](via E83.-): “disorders of mineral metabolism (E83.-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Referenced by Excludes2 notes (13)
- G11 — Hereditary ataxia[Excludes2](via E83.-): “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- G71 — Primary disorders of muscles[Excludes2](via E83.-): “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- K70 — Alcoholic liver disease[Excludes2]: “hemochromatosis (E83.11-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- K70-K77 — Diseases of liver (K70-K77)[Excludes2]: “hemochromatosis (E83.11-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- K71 — Toxic liver disease[Excludes2]: “hemochromatosis (E83.11-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- K72 — Hepatic failure, not elsewhere classified[Excludes2]: “hemochromatosis (E83.11-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- K73 — Chronic hepatitis, not elsewhere classified[Excludes2]: “hemochromatosis (E83.11-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- K74 — Fibrosis and cirrhosis of liver[Excludes2]: “hemochromatosis (E83.11-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- and 5 more
Referenced by Code First instructions
- G63 — Polyneuropathy in diseases classified elsewhere[Code First](via E83.-): “metabolic diseases (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- H42 — Glaucoma in diseases classified elsewhere[Code First](via E83.-): “specified metabolic disorder (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- J84.03 — Idiopathic pulmonary hemosiderosis[Code First](via E83.1.-): “disorders of iron metabolism (E83.1-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
- M14.8 — Arthropathies in other specified diseases classified elsewhere[Code First]: “hemochromatosis (E83.11-)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2026
Nearest codes (39)
- E83 — Disorders of mineral metabolism[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E83.0 — Disorders of copper metabolism[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E83.00 — Disorder of copper metabolism, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E83.01 — Wilson's disease[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E83.09 — Other disorders of copper metabolism[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E83.1 — Disorders of iron metabolism[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E83.10 — Disorder of iron metabolism, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- E83.110 — Hereditary hemochromatosis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- and 31 more
Change history
- FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016
Common coding questions
Can E83.11 be billed directly?
No. E83.11 (Hemochromatosis) is a non-billable ICD-10-CM category code. A more specific billable subcode must be selected based on clinical documentation.
Sources for this page
Codes, titles, notes, index terms and mappings on this page are transcribed from the datasets below. Relationships MedCoder computed and text MedCoder wrote are labelled where they appear.
- Code, title, tabular notes and index terms Official source data
- CMS/CDC ICD-10-CM FY2026 tabular list, index and tables, effective October 1, 2025 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v43.1 (April 2026) Release, file and checksum · Publisher’s page
- Change history and date-of-service validity Official source data
- CMS ICD-10-CM release addenda, ingested release by release into the change ledger Release, file and checksum · Publisher’s page
- Comparisons, relationships and the contextual map MedCoder structured relationship
- Computed by MedCoder from the tabular notes and tables above; every derived relationship is marked as derived where it appears
- Summary and FAQ answers MedCoder explanation
- Written by MedCoder to explain the sources above: drafted with AI assistance, checked by a person against the release files, and labelled as MedCoder text where it appears. Not official text.
Labels on this page: Official source data · MedCoder structured relationship · MedCoder explanation. How to read the labels · All data sources and release dates
Cite this page
Reference this page in a research guide, syllabus or article. The release is included because code content changes each year.
MedCoder.ai. "E83.11 — Hemochromatosis." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/e83.11-hemochromatosis
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionHemochromatosis
No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027 (effective October 1, 2026), and none are recorded for this code. Note changes are tracked from FY2027 only.
Nearest Codes in This Family
Official ICD-10-CM classifications closest to E83.11 in its code family, with their registry titles.
- 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
- E83.110 — Hereditary hemochromatosis
- E83.111 — Hemochromatosis due to repeated red blood cell transfusions
- E83.118 — Other hemochromatosis
- E83.119 — Hemochromatosis, unspecified
- E83.19 — Other disorders of iron metabolism