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G71.13 ICD-10-CM Code: Myotonic chondrodystrophy

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FY 2026 Apr update / Diseases of the nervous system (G00-G99) / Diseases of myoneural junction and muscle (G70-G73)

G71.13

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

Myotonic chondrodystrophy

A rare inherited disorder combining myotonia (muscle stiffness) with skeletal and bone abnormalities, present from birth.

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

0

0

RAF 0

Code Trumping

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Code Book Path

Official
G71Primary disorders of muscles
G71.1Myotonic disorders
G71.13Myotonic chondrodystrophy

Inclusion Terms

Official
  • Chondrodystrophic myotonia
  • Congenital myotonic chondrodystrophy
  • Schwartz-Jampel disease

Excludes 2

Official

ICD-10-CM does not list Excludes 2 notes for G71.13 in this effective period.

Related Child Codes

Official
G71.11Myotonic muscular dystrophy
G71.12Myotonia congenita
G71.14Drug induced myotonia
G71.19Other specified myotonic disorders

Includes

Official

ICD-10-CM does not list Includes notes for G71.13 in this effective period.

Excludes 1

Official

ICD-10-CM does not list Excludes 1 notes for G71.13 in this effective period.

Code First

Official

ICD-10-CM does not list Code First sequencing instructions for G71.13 in this effective period.

Use Additional

Official

ICD-10-CM does not list Use Additional Code instructions for G71.13 in this effective period.

Code Also

Official

ICD-10-CM does not list Code Also instructions for G71.13 in this effective period.

Buddy Documentation Tip

HCC Buddy guidance
This code requires documentation of both myotonic symptoms AND chondrodystrophic features to justify its use
Coordinate with orthopedic documentation to capture the skeletal manifestations for complete clinical picture

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 G71.13 an HCC code?

No. G71.13 is a billable ICD-10-CM code but does not map to any HCC category in V28, V24, ESRD, or RxHCC.

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

G71.13 is the ICD-10-CM diagnosis code for myotonic chondrodystrophy. A rare inherited disorder combining myotonia (muscle stiffness) with skeletal and bone abnormalities, present from birth. G71.13 sits in the ICD-10-CM chapter for diseases of the nervous system (g00-g99), within the section covering diseases of myoneural junction and muscle (g70-g73).

G71.13 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 requires documentation of both myotonic symptoms AND chondrodystrophic features to justify its use.

HCC Buddy maintains structured V28 and V24 mapping, RAF weights, and MEAT documentation criteria for G71.13 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.

Coding Tips

  • This code requires documentation of both myotonic symptoms AND chondrodystrophic features to justify its use
  • Coordinate with orthopedic documentation to capture the skeletal manifestations for complete clinical picture

Child Codes

Code Hierarchy

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