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BC43.20 Nonfamilial restrictive cardiomyopathy

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2025-01

Nonfamilial restrictive cardiomyopathy is restrictive cardiomyopathy secondary to an acquired systemic disorder that is known to be associated with restrictive cardiomyopathy such as amyloidosis, scleroderma, sarcoidosis, or anthracycline therapy.

postcoordination

synonyms

• Nonfamilial restrictive cardiomyopathy
• Secondary restrictive cardiomyopathy
• Restrictive cardiomyopathy due to endomyocardial abnormality
• Endomyocardial cardiomyopathy
• Endomyocardial disease
• Endomyocardial sclerosis
• Endomyocardial fibrosis
• endomyofibrosis (deprecated)
• Tropical endomyocardial fibrosis
• TEMF - [tropical endomyocardial fibrosis]
• EMF - [endomyocardial fibrosis]
• Davies disease
• African endomyocardial fibrosis
• Hypereosinophilic syndrome
• constrictive endocarditis (deprecated)
• Loeffler endocarditis
• Löffler parietal fibroplastic endocarditis
• Endocarditis fibroplastica with eosinophilia
• Endocarditis parietalis fibroplastica
• Fibroplastic parietal endocarditis
• Myocarditis secondary to idiopathic hypereosinophilic syndrome
• Primary eosinophilic Endomyocardial restrictive cardiomyopathy
• Lymphocytic hypereosinophilic syndrome
• Myeloproliferative hypereosinophilic syndrome
• Restrictive cardiomyopathy due to radiation toxicity
• Restrictive cardiomyopathy due to carcinoid syndrome
• Restrictive cardiomyopathy due to scleroderma
• Restrictive cardiomyopathy due to sarcoidosis
• Restrictive cardiomyopathy due to drugs
• Restrictive cardiomyopathy due to anthracycline toxicity
• Wild type transthyretin-related amyloid cardiomyopathy
• senile systemic amyloidosis
• SSA - [senile systemic amyloidosis}
• WTTA - [wild-type transthyretin amyloidosis
• Wild type ATTR - [transthyretin] amyloidosis

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