ICD-10-CM Diagnosis Code I43 - Cardiomyopathy in diseases classified elsewhere (original) (raw)
ICD List 2025-2026 Edition
- Home
- ICD-10-CM Codes
- I00–I99
- I30-I5A
- I43
- 2026 ICD-10-CM Code I43
Cardiomyopathy in diseases classified elsewhere
ICD-10-CM Code:
I43
ICD-10 Code for:
Cardiomyopathy in diseases classified elsewhere
Is Billable?
Yes - Valid for Submission
Chronic Condition Indicator: [1]
Chronic
Code Navigator:
I43 is a billable diagnosis code used to specify a medical diagnosis of cardiomyopathy in diseases classified elsewhere. The code is valid during the current fiscal year for the submission of HIPAA-covered transactions from October 01, 2025 through September 30, 2026.
- Code Information
- Approximate Synonyms
- Clinical Classification
- Clinical Information
- Tabular List of Diseases and Injuries
- Code Edits
- Diagnostic Related Groups Mapping
- Convert to ICD-9 Code
- Patient Education
- Code History
- Diseases of the circulatory system
I00–I99
The following list of clinical terms are approximate synonyms, alternative descriptions, or common phrases that might be used by patients, healthcare providers, or medical coders to describe the same condition. These synonyms and related diagnosis terms are often used when searching for an ICD-10 code, especially when the exact medical terminology is unclear. Whether you're looking for lay terms, similar diagnosis names, or common language alternatives, this list can help guide you to the correct ICD-10 classification.
- Acromegalic cardiomyopathy
- Cardiac familial non-neuropathic amyloidosis
- Cardiac familial non-neuropathic amyloidosis
- Cardiac glycogen phosphorylase kinase deficiency
- Cardiac secondary systemic amyloidosis
- Cardiomyopathy associated with another disorder
- Cardiomyopathy due to connective tissue disease
- Cardiomyopathy due to connective tissue disease
- Cardiomyopathy due to COVID-19
- Cardiomyopathy due to storage disease
- Cardiomyopathy due to viral infection
- Cardiomyopathy in Duchenne muscular dystrophy
- Cardiomyopathy in Friedreich's ataxia
- Cardiomyopathy in myotonic dystrophy
- Diabetic cardiomyopathy
- Dilated cardiomyopathy due to systemic lupus erythematosus
- Disorder of heart due to systemic lupus erythematosus
- Endomyocardial fibrosis
- Familial cardiomyopathy
- Familial cardiomyopathy
- Familial non-neuropathic amyloidosis
- Familial non-neuropathic amyloidosis
- Familial restrictive cardiomyopathy
- Familial restrictive cardiomyopathy
- Glycogen phosphorylase kinase deficiency
- Glycogen phosphorylase kinase deficiency, autosomal recessive
- Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
- Heart disease due to thyrotoxicosis
- Hereditary ATTR amyloidosis
- Infiltrative cardiomyopathy
- Localized hereditary amyloidosis
- Localized hereditary cardiac amyloidosis
- Primary eosinophilic endomyocardial cardiomyopathy
- Primary eosinophilic endomyocardial restrictive cardiomyopathy
- Primary restrictive cardiomyopathy
- Primary triglyceride deposit cardiomyovasculopathy
- Restrictive cardiomyopathy secondary to familial storage disease
- Restrictive cardiomyopathy with endomyocardial fibrosis
- Secondary systemic amyloidosis
- Thyrotoxic cardiomyopathy
- Transthyretin related familial amyloid cardiomyopathy
Clinical Classifications group individual ICD-10-CM diagnosis codes into broader, clinically meaningful categories. These categories help simplify complex data by organizing related conditions under common clinical themes.
They are especially useful for data analysis, reporting, and clinical decision-making. Even when diagnosis codes differ, similar conditions can be grouped together based on their clinical relevance. Each category is assigned a unique CCSR code that represents a specific clinical concept, often tied to a body system or medical specialty.
CCSR Code: CIR005
Inpatient Default: X - Not applicable.
Outpatient Default: X - Not applicable.
Endomyocardial Fibrosis
a condition characterized by the thickening of the ventricular endocardium and subendocardium (myocardium), seen mostly in children and young adults in the tropical climate. the fibrous tissue extends from the apex toward and often involves the heart valves causing restrictive blood flow into the respective ventricles (cardiomyopathy, restrictive).
Endomyocardial Fibrosis
a disease characterized by fibrotic thickening of the endocardium, particularly the right and/or left inflow tracts. the disease often involves the atrioventricular valves, leading to valvular regurgitaion. it most commonly occurs in children living within 15 degrees of the equator.
Myocardial Degeneration
degeneration of myocardial tissue.
The Medicare Code Editor (MCE) detects errors and inconsistencies in ICD-10-CM diagnosis coding that can affect Medicare claim validity. These Medicare code edits help medical coders and billing professionals determine when a diagnosis code is not appropriate as a principal diagnosis, does not meet coverage criteria. Use this list to verify whether a code is valid for Medicare billing and to avoid claim rejections or denials due to diagnosis coding issues.
Manifestation codes describe the manifestation of an underlying disease, not the disease itself, and therefore should not be used as a principal diagnosis.
Below are the ICD-9 codes that most closely match this ICD-10 code, based on the General Equivalence Mappings (GEMs). This ICD-10 to ICD-9 crosswalk tool is helpful for coders who need to reference legacy diagnosis codes for audits, historical claims, or approximate code comparisons.
ICD-9-CM: 425.8
Approximate Flag - The approximate mapping means this ICD-10 code does not have an exact ICD-9 equivalent. The matched code is the closest available option, but it may not fully capture the original diagnosis or clinical intent.
Cardiomyopathy
Cardiomyopathy is the name for diseases of the heart muscle. These diseases enlarge your heart muscle or make it thicker and more rigid than normal. In rare cases, scar tissue replaces the muscle tissue.
Some people live long, healthy lives with cardiomyopathy. Some people don't even realize they have it. In others, however, it can make the heart less able to pump blood through the body. This can cause serious complications, including:
- Heart failure
- Abnormal heart rhythms
- Heart valve problems
- Sudden cardiac arrest (SCA)
Heart attacks, high blood pressure, infections, and other diseases can all cause cardiomyopathy. Some types of cardiomyopathy run in families. In many people, however, the cause is unknown. Treatment might involve medicines, surgery, other medical procedures, and lifestyle changes.
NIH: National Heart, Lung, and Blood Institute
FY 2026 - No Change, effective from 10/1/2025 through 9/30/2026
FY 2025 - No Change, effective from 10/1/2024 through 9/30/2025
FY 2024 - No Change, effective from 10/1/2023 through 9/30/2024
FY 2023 - No Change, effective from 10/1/2022 through 9/30/2023
FY 2022 - No Change, effective from 10/1/2021 through 9/30/2022
FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021
FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016. This was the first year ICD-10-CM was implemented into the HIPAA code set.
