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)
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- systemic connective tissue disorders (M30-M36)
- transient cerebral ischemic attacks and related syndromes (G45.-)
Code First
The underlying condition must be sequenced before this code
- underlying disease, such as:
- amyloidosis (E85.-)
- glycogen storage disease (E74.0-)
- gout (M10.0-)
- thyrotoxicosis (E05.0-E05.9-)
Also Known As / Clinical Terms
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
Frequently Asked Questions
What is ICD-10 code I43?
ICD-10-CM code I43 represents "Cardiomyopathy in diseases classified elsewhere". It 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.
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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.