Diagnosis Code

I43 CARDIOMYOPATHY IN DISEASES CLASSIFIED ELSEWHERE


Code Information

Diagnosis Code: I43

Short Description: Cardiomyopathy in diseases classified elsewhere

Long Description: Cardiomyopathy in diseases classified elsewhere

The code I43 is VALID for claim submission

Code Classification:

  • Diseases of the circulatory system (I00–I99)
    • Other forms of heart disease (I30-I5A)
      • Cardiomyopathy in diseases classified elsewhere (I43)
        • I43 Cardiomyopathy in diseases classified elsewhere

This code is valid for manifestation diagnoses

Code Version: 2022 ICD-10-CM


Synonyms

  • 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
  • Infiltrative cardiomyopathy
  • Localized hereditary amyloidosis
  • Localized hereditary cardiac amyloidosis
  • Myocardial degeneration
  • Primary eosinophilic endomyocardial cardiomyopathy
  • Primary eosinophilic endomyocardial restrictive cardiomyopathy
  • Primary restrictive cardiomyopathy
  • Restrictive cardiomyopathy secondary to familial storage disease
  • Restrictive cardiomyopathy with endomyocardial fibrosis
  • Secondary systemic amyloidosis
  • Thyrotoxic cardiomyopathy
  • Transthyretin related familial amyloid cardiomyopathy

Diagnostic Related Group(s)

The code I43 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)
  • Other Circulatory System Diagnoses With Mcc (314)
  • Other Circulatory System Diagnoses With Cc (315)
  • Other Circulatory System Diagnoses Without Cc/mcc (316)

References to Index of Diseases and Injuries

The code I43 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Type 1 Excludes Notes:
    • cardiomyopathy (in):
    • coxsackie (virus) (@B33.24*)
    • diphtheria (@A36.81*)
    • sarcoidosis (@D86.85*)
    • tuberculosis (@A18.84*)
  • Code First:
    • underlying disease, such as:
    • amyloidosis (@E85*.-)
    • glycogen storage disease (@E74.0*-)
    • gout (@M10.0*-)
    • thyrotoxicosis (@E05.0*[email protected]*-)

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
I43 Right Arrow 425.8 Cardiomyopath in oth dis

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description


This page was last updated on: 10/1/2023