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I42.1 ICD-10-CM Code: Obstructive hypertrophic cardiomyopathy

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FY 2026 Apr update / Diseases of the circulatory system (I00-I99) / Other forms of heart disease (I30-I5A)

I42.1

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

Obstructive hypertrophic cardiomyopathy

A condition where the heart muscle becomes abnormally thick, particularly in the wall between the two lower chambers, which can obstruct blood flow out of the heart.

Buddy the Bee presenting code insight

Buddy Insight

Obstructive hypertrophic cardiomyopathy is a genetic heart condition causing asymmetric thickening of the interventricular septum that obstructs left ventricular outflow.

CMS-HCC V28

HCC 227

RAF 0.339

CMS-HCC V24

HCC 85

RAF 0.368

ACA/HHS

0

0

RAF 0

ESRD/PACE

HCC 85

RAF 0.0

RXHCC

HCC 186

RAF 0.0

Code Trumping

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Code Book Path

Official
I42Cardiomyopathy
I42.1Obstructive hypertrophic cardiomyopathy

Inclusion Terms

Official
  • Hypertrophic subaortic stenosis (idiopathic)

Excludes 2

Official
  • ischemic cardiomyopathy (I25.5)
  • peripartum cardiomyopathy (O90.3)
  • ventricular hypertrophy (I51.7)

Related Child Codes

Official
I42.0Dilated cardiomyopathy
I42.2Other hypertrophic cardiomyopathy
I42.3Endomyocardial (eosinophilic) disease
I42.4Endocardial fibroelastosis
I42.5Other restrictive cardiomyopathy

Includes

Official
  • myocardiopathy

Excludes 1

Official

ICD-10-CM does not list Excludes 1 notes for I42.1 in this effective period.

Code First

Official
  • pre-existing cardiomyopathy complicating pregnancy and puerperium (O99.4)

Use Additional

Official

ICD-10-CM does not list Use Additional Code instructions for I42.1 in this effective period.

Code Also

Official

ICD-10-CM does not list Code Also instructions for I42.1 in this effective period.

Buddy Documentation Tip

HCC Buddy guidance
Provider diagnosis of obstructive hypertrophic cardiomyopathy
Echocardiographic findings showing asymmetric septal hypertrophy with left ventricular outflow tract obstruction
Left ventricular outflow tract gradient documented
Family history of hypertrophic cardiomyopathy or sudden cardiac death

MEAT Support

HCC Buddy guidance
Provider diagnosis of obstructive hypertrophic cardiomyopathy
Echocardiographic findings showing asymmetric septal hypertrophy with left ventricular outflow tract obstruction
Left ventricular outflow tract gradient documented
Family history of hypertrophic cardiomyopathy or sudden cardiac death

Audit Caution

HCC Buddy guidance
Confusing obstructive with non-obstructive hypertrophic cardiomyopathy — the obstruction distinction is critical (I42.1 vs I42.2)
Coding hypertensive heart disease as hypertrophic cardiomyopathy — these are different conditions
Not coding associated arrhythmias or complications separately
Failing to document the obstruction gradient, which differentiates I42.1 from I42.2

Common Mistakes

HCC Buddy guidance
I42.2 — Other hypertrophic cardiomyopathy; non-obstructive form without outflow tract obstruction
I42.0 — Dilated cardiomyopathy; enlarged and weakened heart, not thickened
I11.0 — Hypertensive heart disease with heart failure; hypertensive cardiac hypertrophy is different
I42.9 — Cardiomyopathy, unspecified; use only when the type is not documented

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 I42.1 an HCC code?

Yes. I42.1 maps to Cardiomyopathy under the CMS-HCC V28 risk adjustment model (and Congestive Heart Failure under V24).

HCC Category Mapping

V28HCC 227, Cardiomyopathy
0.339
V24HCC 85, Congestive Heart Failure
0.368
ESRDHCC 85, Congestive Heart Failure
0.000
RxHCCHCC 186, Heart Failure
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 I42.1

For I42.1to 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 I42.1 during that encounter, not just copy-forwarded from a problem list.

What This Code Means

I42.1 is the ICD-10-CM diagnosis code for obstructive hypertrophic cardiomyopathy. A condition where the heart muscle becomes abnormally thick, particularly in the wall between the two lower chambers, which can obstruct blood flow out of the heart. I42.1 sits in the ICD-10-CM chapter for diseases of the circulatory system (i00-i99), within the section covering other forms of heart disease (i30-i5a).

Under the CMS-HCC V28 risk adjustment model, I42.1 maps to Cardiomyopathy (HCC 227) with a community, non-dual, aged base RAF weight of 0.339. Under the older CMS-HCC V24 model, I42.1 maps to Congestive Heart Failure (HCC 85) with a community, non-dual, aged base RAF weight of 0.368. V28 is the CMS-HCC risk adjustment model that reached 100% phase-in for payment year 2026, replacing V24 which was used during the PY2024–PY2025 transition.

Document whether the patient has symptoms such as chest pain, shortness of breath, or syncope. Because I42.1 maps to a payment HCC, the provider's documentation must satisfy MEAT criteria (Monitor, Evaluate, Assess, or Treat) for the encounter to count toward the patient's Medicare Advantage risk adjustment score. When documentation is ambiguous, coders should issue a provider query rather than assume the highest-specificity variant.

HCC Buddy maintains structured V28 and V24 mapping, RAF weights, and MEAT documentation criteria for I42.1 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.

Coding Tips

  • Document whether the patient has symptoms such as chest pain, shortness of breath, or syncope
  • Note any family history of sudden cardiac death or hypertrophic cardiomyopathy

Clinical Significance

Obstructive hypertrophic cardiomyopathy is a genetic heart condition causing asymmetric thickening of the interventricular septum that obstructs left ventricular outflow. It is the most common cause of sudden cardiac death in young athletes. This condition requires lifelong monitoring, activity restrictions, and may necessitate septal reduction therapy or implantable cardioverter defibrillator placement.

Documentation Requirements

  • Provider diagnosis of obstructive hypertrophic cardiomyopathy
  • Echocardiographic findings showing asymmetric septal hypertrophy with left ventricular outflow tract obstruction
  • Left ventricular outflow tract gradient documented
  • Family history of hypertrophic cardiomyopathy or sudden cardiac death
  • Symptoms (exertional dyspnea, syncope, chest pain) and functional status

Commonly Confused Codes

  • I42.2: Other hypertrophic cardiomyopathy; non-obstructive form without outflow tract obstruction
  • I42.0: Dilated cardiomyopathy; enlarged and weakened heart, not thickened
  • I11.0: Hypertensive heart disease with heart failure; hypertensive cardiac hypertrophy is different
  • I42.9: Cardiomyopathy, unspecified; use only when the type is not documented

Child Codes

Code Hierarchy

I42CardiomyopathyI42.1Obstructive hypertrophic cardiomyopathy
I42.1Obstructive hypertrophic cardiomyopathy

More on I42.1

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