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E83.119 ICD-10-CM Code: Hemochromatosis, unspecified

ICD-10-CM Code View

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FY 2026 Apr update / Endocrine, nutritional and metabolic diseases (E00-E89) / Metabolic disorders (E70-E88)

E83.119

Billable / SpecificICD-10-CMOfficial ICD-10-CMCodebook guidance

Hemochromatosis, unspecified

Iron overload in the body when the specific type or cause is not documented or determined.

Buddy the Bee presenting code insight

Buddy Insight

Hemochromatosis, unspecified is used when iron overload is confirmed but the specific type (hereditary vs.

CMS-HCC V28

0

0

RAF 0

CMS-HCC V24

0

0

RAF 0

ACA/HHS

0

0

RAF 0

ESRD/PACE

0

0

RAF 0

RXHCC

HCC 43

RAF 0.0

Code Trumping

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Code Book Path

Official
E83.1Disorders of iron metabolism
E83.11Hemochromatosis
E83.119Hemochromatosis, unspecified

Inclusion Terms

Official

ICD-10-CM does not list inclusion terms for E83.119 in this effective period.

Excludes 2

Official

ICD-10-CM does not list Excludes 2 notes for E83.119 in this effective period.

Related Child Codes

Official
E83.110Hereditary hemochromatosis
E83.111Hemochromatosis due to repeated red blood cell transfusions
E83.118Other hemochromatosis

Includes

Official

ICD-10-CM does not list Includes notes for E83.119 in this effective period.

Excludes 1

Official
  • GALD (P78.84)
  • Gestational alloimmune liver disease (P78.84)
  • Neonatal hemochromatosis (P78.84)

Code First

Official

ICD-10-CM does not list Code First sequencing instructions for E83.119 in this effective period.

Use Additional

Official

ICD-10-CM does not list Use Additional Code instructions for E83.119 in this effective period.

Code Also

Official

ICD-10-CM does not list Code Also instructions for E83.119 in this effective period.

Buddy Documentation Tip

HCC Buddy guidance
Diagnosis of hemochromatosis by the treating provider
Laboratory evidence of iron overload (elevated ferritin, transferrin saturation)
Reason the type cannot be specified (pending genetic testing, new diagnosis workup)
Treatment plan or referral for further evaluation

MEAT Support

HCC Buddy guidance
Diagnosis of hemochromatosis by the treating provider
Laboratory evidence of iron overload (elevated ferritin, transferrin saturation)
Reason the type cannot be specified (pending genetic testing, new diagnosis workup)
Treatment plan or referral for further evaluation

Audit Caution

HCC Buddy guidance
Accepting the unspecified code when documentation actually supports hereditary type — always review for genetic testing results or family history
Missing HCC capture opportunity by not querying provider to specify hereditary vs. other type
Using this code when 'elevated ferritin' or 'iron overload' is documented without a formal hemochromatosis diagnosis
Not recognizing that clarification between hereditary and other forms directly impacts risk adjustment

Common Mistakes

HCC Buddy guidance
E83.110 — Hereditary hemochromatosis: preferred code when hereditary type is confirmed; carries HCC mapping
E83.118 — Other hemochromatosis: use when secondary or non-hereditary type is specified
E83.10 — Disorder of iron metabolism, unspecified: even less specific; avoid if hemochromatosis is documented
R79.89 — Other specified abnormal findings of blood chemistry: do not use for elevated ferritin when hemochromatosis is diagnosed

Last updated: FY2026 ICD-10-CM Apr update, Apr 1, 2026 through Sep 30, 2026. CMS-HCC V28 is 100% phased in for payment year 2026.

Is E83.119 an HCC code?

No. E83.119 is a billable ICD-10-CM code but does not map to any HCC category in V28, V24, ESRD, or RxHCC.

HCC Category Mapping

RxHCCHCC 43, Other Significant Endocrine and Metabolic Disorders
0.000

RAF weights shown are the community, non-dual, aged base weights from the CMS risk adjustment model file. Actual per-patient RAF contribution depends on member segment, interactions, and the model year used by the payer. V28 is the CMS-HCC model phased in over payment years 2024–2026; V24 remains in use during the transition and for historical data.

MEAT Criteria for E83.119

For E83.119to count as a valid HCC diagnosis in a given encounter, the provider's documentation must show MEAT: Monitor, Evaluate, Assess, or Treat. A diagnosis from a prior year does not carry forward automatically, it has to be re-documented and supported each calendar year.

  • MMonitor: signs, symptoms, disease progression, or lab trending documented in the note
  • EEvaluate: test results, medication response, or physical findings reviewed by the provider
  • AAssess: explicit mention in the assessment or plan with acknowledgment of status
  • TTreat: medication, referral, procedure, therapy, or counseling tied to the diagnosis

Only one of M/E/A/T is required to support the code, but the documentation must be specific enough to show that the provider actually addressed E83.119 during that encounter, not just copy-forwarded from a problem list.

What This Code Means

E83.119 is the ICD-10-CM diagnosis code for hemochromatosis, unspecified. Iron overload in the body when the specific type or cause is not documented or determined. E83.119 sits in the ICD-10-CM chapter for endocrine, nutritional and metabolic diseases (e00-e89), within the section covering metabolic disorders (e70-e88).

E83.119 is a billable ICD-10-CM code but does not map to a payment HCC under the CMS-HCC V28, V24, ESRD, or RxHCC risk adjustment models. It can be reported on Medicare Advantage encounter data submissions but it does not contribute to a beneficiary's RAF score and therefore does not affect risk-adjusted payments to the plan.

This code does NOT map to a CMS-HCC under V24 or V28 models. It maps only to RxHCC 43. If the provider can confirm hereditary hemochromatosis, E83.110 should be used instead to capture V24 HCC 23 (RAF 0.23). This is a high-value query opportunity.

HCC Buddy maintains structured V28 and V24 mapping, RAF weights, and MEAT documentation criteria for E83.119 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.

Coding Tips

  • This is a less specific code; query the provider if the type of hemochromatosis can be determined
  • Use only when documentation does not specify hereditary or secondary causes

Clinical Significance

Hemochromatosis, unspecified is used when iron overload is confirmed but the specific type (hereditary vs. acquired) has not been determined. This code should prompt a query to the provider for clarification, as hereditary hemochromatosis maps to an HCC while this unspecified code does not.

Documentation Requirements

  • Diagnosis of hemochromatosis by the treating provider
  • Laboratory evidence of iron overload (elevated ferritin, transferrin saturation)
  • Reason the type cannot be specified (pending genetic testing, new diagnosis workup)
  • Treatment plan or referral for further evaluation
  • Query attempt to provider for hereditary vs. acquired specification

Commonly Confused Codes

  • E83.110: Hereditary hemochromatosis: preferred code when hereditary type is confirmed; carries HCC mapping
  • E83.118: Other hemochromatosis: use when secondary or non-hereditary type is specified
  • E83.10: Disorder of iron metabolism, unspecified: even less specific; avoid if hemochromatosis is documented
  • R79.89: Other specified abnormal findings of blood chemistry: do not use for elevated ferritin when hemochromatosis is diagnosed

Child Codes

Code Hierarchy

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