I43
BillableCardiomyopathy in diseases classified elsewhere
Cardiomyopathy in diseases classified elsewhere
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- cardiomyopathy (in):
- •coxsackie (virus)B33.24
- •diphtheriaA36.81
- •sarcoidosisD86.85
- •tuberculosisA18.84
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •systemic connective tissue disordersM30-M36
- •transient cerebral ischemic attacks and related syndromesG45
Code First
The underlying condition must be sequenced before this code
- underlying disease, such as:
- •amyloidosisE85
- •glycogen storage diseaseE74.0
- •goutM10.0
- •thyrotoxicosis-)E05.0-E05.9
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(167)
SNOMED CT
- Restrictive cardiomyopathy secondary to familial storage disease30884007
- Constrictive endocarditis33258008
- Eosinophilic endomyocardial disease33258008
- Löffler's endocarditis33258008
- Löffler's parietal fibroplastic endocarditis33258008
- Primary eosinophilic endomyocardial restrictive cardiomyopathy33258008
- Familial cardiomyopathy35728003
- Primary familial cardiomyopathy35728003
- Dilated cardiomyopathy due to systemic lupus erythematosus36471000
- Primary eosinophilic endomyocardial cardiomyopathy53703001
- Primary restrictive cardiomyopathy90828009
- Cardiomyopathy associated with another disorder195029002
- Cardiomyopathy, secondary195029002
- Secondary cardiomyopathy195029002
- Cardiomyopathy in Friedreich ataxia195030007
- Cardiomyopathy in Friedreich's ataxia195030007
- Cardiomyopathy in myotonic dystrophy195031006
- Familial restrictive cardiomyopathy233878008
- Glycogen phosphorylase kinase deficiency235908005
- Glycogen storage disease type IX235908005
- Glycogenosis viiia235908005
- Hepatic phosphorylase kinase deficiency235908005
- PHK - Hepatic phosphorylase kinase deficiency235908005
- Phosphorylase kinase deficiency of liver235908005
- Familial non-neuropathic amyloidosis237868006
- Nonneuropathic heredofamilial amyloidosis237868006
- Localised hereditary amyloidosis237869003
- Localized hereditary amyloidosis237869003
- Organ limited hereditary amyloidosis237869003
- Glycogen phosphorylase kinase deficiency, autosomal recessive297252005
- Cardiac glycogen phosphorylase kinase deficiency297253000
- Cardiomyopathy in Duchenne muscular dystrophy315608004
- Endomyocardial fibrosis398716006
- Endomyocardial sclerosis398716006
- Idiopathic mural endomyocardial disease398716006
- African endomyocardial fibrosis398754006
- Obscure African cardiomyopathy398754006
- Obscure cardiomyopathy of Africa398754006
- Restrictive cardiomyopathy with endomyocardial fibrosis398754006
- ATTRV122I amyloidosis715655000
- Transthyretin amyloid cardiopathy715655000
- Transthyretin related familial amyloid cardiomyopathy715655000
- Glycogen storage disease type 15717821004
- Glycogen storage disease type XV717821004
- Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency717821004
- Glycogenosis with severe cardiomyopathy due to glycogenin deficiency717821004
- Cardiomyopathy due to diabetes mellitus788878000
- Diabetic cardiomyopathy788878000
- Secondary systemic amyloidosis858580008
- Cardiomyopathy due to connective tissue disease860837007
- Cardiomyopathy due to storage disease860839005
- Infiltrative cardiomyopathy871646007
- Heart disease due to thyrotoxicosis1003678001
- Cardiomyopathy due to thyrotoxicosis1137377003
- Thyrotoxic cardiomyopathy1137377003
- Disorder of heart due to systemic lupus erythematosus1144921004
- Acromegalic cardiomyopathy1186866009
- Cardiomyopathy due to acromegaly1186866009
- Cardiac familial non-neuropathic amyloidosis1187147003
- Familial non-neuropathic amyloidosis of heart1187147003
- Localised hereditary amyloidosis of heart1187149000
- Localised hereditary cardiac amyloidosis1187149000
- Localized hereditary amyloidosis of heart1187149000
- Localized hereditary cardiac amyloidosis1187149000
- Cardiac secondary systemic amyloidosis1187540008
- Secondary systemic amyloidosis of heart1187540008
- Neutral lipid storage disease with severe cardiovascular involvement1279844009
- Primary triglyceride deposit cardiomyovasculopathy1279844009
- ATTRv amyloidosis1354544003
- Familial TTR-related amyloidosis1354544003
- Familial transthyretin-related amyloidosis1354544003
- Hereditary ATTR amyloidosis1354544003
- Hereditary TTR amyloid polyneuropathy1354544003
- Hereditary TTR amyloidosis1354544003
- Hereditary transthyretin amyloid polyneuropathy1354544003
- Hereditary transthyretin related amyloidosis1354544003
- hATTR - hereditary transthyretin related amyloidosis1354544003
- Cardiomyopathy due to COVID-19119731000146105
- Cardiomyopathy due to disease caused by 2019 novel coronavirus119731000146105
- Cardiomyopathy due to disease caused by 2019-nCoV119731000146105
- Cardiomyopathy due to disease caused by SARS-CoV-2119731000146105
- Cardiomyopathy due to disease caused by severe acute respiratory syndrome coronavirus 2119731000146105
- Cardiomyopathy due to viral infection204981000119101
Clinical Terms
- Cardiomyopathy due to disease caused by severe acute respiratory syndrome coronavirus 2
- Cardiomyopathy due to disease caused by SARS-CoV-2
- Endomyocardial fibrosis
- Thyrotoxic cardiomyopathy
- Glycogen phosphorylase kinase deficiency, autosomal recessive
- Glycogenosis viiia
- Hepatic phosphorylase kinase deficiency
- Primary familial cardiomyopathy
- Cardiomyopathy due to thyrotoxicosis
- Familial cardiomyopathy
- Cardiomyopathy due to connective tissue disease
- Glycogen phosphorylase kinase deficiency
- Phosphorylase kinase deficiency of liver
- Familial restrictive cardiomyopathy
- Secondary cardiomyopathy
- Obscure cardiomyopathy of Africa
- Familial non-neuropathic amyloidosis of heart
- Cardiomyopathy, secondary
- Cardiomyopathy due to diabetes mellitus
- Hereditary TTR amyloidosis
- Infiltrative cardiomyopathy
- Glycogen storage disease type 15
- Organ limited hereditary amyloidosis
- Hereditary TTR amyloid polyneuropathy
- Constrictive endocarditis
- Glycogen storage disease type IX
- Localized hereditary amyloidosis
- Cardiomyopathy associated with another disorder
- Localized hereditary amyloidosis of heart
- Localised hereditary amyloidosis of heart
- Cardiomyopathy in Duchenne muscular dystrophy
- Restrictive cardiomyopathy with endomyocardial fibrosis
- Cardiomyopathy due to disease caused by 2019-nCoV
- Disorder of heart due to systemic lupus erythematosus
- Hereditary transthyretin related amyloidosis
- Familial TTR-related amyloidosis
- Cardiomyopathy due to viral infection
- Obscure African cardiomyopathy
- Secondary systemic amyloidosis of heart
- Cardiomyopathy in Friedreich ataxia
- Hereditary ATTR amyloidosis
- Endomyocardial sclerosis
- Nonneuropathic heredofamilial amyloidosis
- Glycogen storage disease type XV
- Primary triglyceride deposit cardiomyovasculopathy
- Secondary systemic amyloidosis
- PHK - Hepatic phosphorylase kinase deficiency
- Transthyretin amyloid cardiopathy
- Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
- Restrictive cardiomyopathy secondary to familial storage disease
- Localised hereditary amyloidosis
- Localised hereditary cardiac amyloidosis
- ATTRv amyloidosis
- African endomyocardial fibrosis
- Idiopathic mural endomyocardial disease
- Cardiomyopathy due to storage disease
- Diabetic cardiomyopathy
- Eosinophilic endomyocardial disease
- Cardiac secondary systemic amyloidosis
- hATTR - hereditary transthyretin related amyloidosis
- Cardiomyopathy in myotonic dystrophy
- Hereditary transthyretin amyloid polyneuropathy
- Familial non-neuropathic amyloidosis
- Localized hereditary cardiac amyloidosis
- Cardiac glycogen phosphorylase kinase deficiency
- Familial transthyretin-related amyloidosis
- Löffler's parietal fibroplastic endocarditis
- Löffler's endocarditis
- Primary eosinophilic endomyocardial restrictive cardiomyopathy
- Transthyretin related familial amyloid cardiomyopathy
- Acromegalic cardiomyopathy
- Cardiomyopathy due to disease caused by 2019 novel coronavirus
- ATTRV122I amyloidosis
- Primary eosinophilic endomyocardial cardiomyopathy
- Neutral lipid storage disease with severe cardiovascular involvement
- Primary restrictive cardiomyopathy
- Dilated cardiomyopathy due to systemic lupus erythematosus
- Heart disease due to thyrotoxicosis
- Cardiac familial non-neuropathic amyloidosis
- Cardiomyopathy due to acromegaly
- Cardiomyopathy due to COVID-19
- Cardiomyopathy in Friedreich's ataxia
- Glycogenosis with severe cardiomyopathy due to glycogenin deficiency
Frequently Asked Questions
What is the ICD-10 code for cardiomyopathy in diseases classified elsewhere?
The ICD-10-CM code for cardiomyopathy in diseases classified elsewhere is I43. The full clinical description is "Cardiomyopathy in diseases classified elsewhere". I43 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code I43 mean?
ICD-10-CM code I43 represents “Cardiomyopathy in diseases classified elsewhere”. It is classified under Chapter 9: Diseases of the Circulatory System and is a billable/specific code that can be used on a claim.
Is I43 a billable code?
Yes, I43 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is I43 in?
I43 is in Chapter 9: Diseases of the Circulatory System (codes I00-I99).
What codes cannot be used with I43?
I43 has Excludes1 notes indicating codes that cannot be used together with it, including: cardiomyopathy (in):; coxsackie (virus) (B33.24); diphtheria (A36.81); and 2 more.
What SNOMED CT codes does I43 map to?
I43 maps to 36 SNOMED CT concepts: 715655000, 1354544003, 1186866009, 398754006, 1187147003, and 31 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for I43?
I43 is linked to 1 UMLS Concept Unique Identifier: C0694499. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does I43 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like cardiomyopathy in diseases classified elsewhere affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of I43?
I43 maps to the ICD-11 code: BC43.Z (Cardiomyopathy, unspecified).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.