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E88.82 ICD-10-CM Code: Obesity due to disruption of MC4R pathway

E88.82 is not a CMS-HCC payment code. MEAT criteria · RAF Calculator · HCC Buddy coding tools

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Code lookupE88.82

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

E88.82

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

Obesity due to disruption of MC4R pathway

Obesity caused by a genetic defect in the MC4R pathway, which controls appetite and energy expenditure in the brain.

CMS-HCC V28

N/A

Not mapped

CMS-HCC V24

Historical

Historical

Not used for CY2026 payment

ACA/HHS

N/A

Not mapped

ESRD/PACE

N/A

Not mapped

RXHCC

N/A

Not mapped

Inclusion Terms

Official

No inclusion terms are included in this display for E88.82. Check the code and parent instructions in the Code Book.

Excludes 2

Official
  • Ehlers-Danlos syndromes (Q79.6-)Inherited from E70-E88

Includes

Official

No Includes notes are included in this display for E88.82. Check the code and parent instructions in the Code Book.

Excludes 1

Official
  • transitory endocrine and metabolic disorders specific to newborn (P70-P74)Inherited from E00-E89, E70-E88, E88
  • androgen insensitivity syndrome (E34.5-)Inherited from E00-E89, E70-E88, E88
  • congenital adrenal hyperplasia (E25.0)Inherited from E00-E89, E70-E88, E88
  • hemolytic anemias attributable to enzyme disorders (D55.-)Inherited from E00-E89, E70-E88, E88
  • Marfan syndrome (Q87.4-)Inherited from E00-E89, E70-E88, E88
  • 5-alpha-reductase deficiency (E29.1)Inherited from E00-E89, E70-E88, E88
  • histiocytosis X (chronic) (C96.6)Inherited from E00-E89, E70-E88, E88

Code First

Official

No Code First sequencing instructions are included in this display for E88.82. Check the code and parent instructions in the Code Book.

Use Additional

Official
  • code, if applicable, to identify associated manifestations, such as polyphagia (R63.2)
  • code to identify body mass index (BMI), if known (Z68.-)
  • codes for associated conditionsInherited from E88

Code Also

Official

No Code Also instructions are included in this display for E88.82. Check the code and parent instructions in the Code Book.

Buddy Documentation Tip

HCC Buddy guidance
This code requires documented genetic testing or clinical evidence of MC4R pathway disruption; do not use for common obesity
Code the obesity severity (E66.0-E66.9) in addition to this code to fully capture the clinical picture

Current with CMS: FY2026 ICD-10-CM Apr 1 update (effective Apr 1 – Sep 30, 2026) · CMS-HCC V28, 100% phased in for payment year 2026. FY2027 code set already staged for October 1, 2026. How HCC Buddy stays current →

Is E88.82 an HCC code?

No. E88.82 is a billable ICD-10-CM code with no mapping under the CMS-HCC V28 or V24 community payment models, and none under the ESRD, Part D RxHCC, or HHS-HCC models.

Code
E88.82
Description
Obesity due to disruption of MC4R pathway
HCC (V28)
No CMS-HCC V28 mapping
RAF reference coefficient
Billable
Yes
Payment year
2026

Coder workflow notes

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This code does not map to an HCC category in any model (V28, V24, ESRD, RxHCC).

What This Code Means

E88.82 is the ICD-10-CM diagnosis code for obesity due to disruption of mc4r pathway. Obesity caused by a genetic defect in the MC4R pathway, which controls appetite and energy expenditure in the brain. E88.82 sits in the ICD-10-CM chapter for endocrine, nutritional and metabolic diseases (e00-e89), within the section covering metabolic disorders (e70-e88).

E88.82 is a billable ICD-10-CM code, but the current payload does not show a mapping under the CMS-HCC V28 or V24 community payment models, and none under the ESRD, Part D RxHCC, or HHS-HCC models. Do not assign risk adjustment value from this page when no source-backed mapping is shown; verify the applicable model and payment year.

This code requires documented genetic testing or clinical evidence of MC4R pathway disruption; do not use for common obesity.

HCC Buddy maintains structured V28 and V24 mapping, source-labeled coefficient references, and MEAT documentation criteria for E88.82 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.

Coding Tips

  • This code requires documented genetic testing or clinical evidence of MC4R pathway disruption; do not use for common obesity
  • Code the obesity severity (E66.0-E66.9) in addition to this code to fully capture the clinical picture

Use Additional Code

  • code, if applicable, to identify associated manifestations, such as polyphagia (R63.2)
  • code to identify body mass index (BMI), if known (Z68.-)

Child Codes

Code Hierarchy

E88.82 code history

Code setChange
FY2025 (effective Oct 1, 2024)Added to the code set

Source: official CMS ICD-10-CM order and addenda files, FY2016 through FY2027.

More on E88.82

Referenced in blog posts

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