I42.8
BillableOther cardiomyopathies
Other cardiomyopathies
Coding Notes
Includes
Conditions included under this code
- myocardiopathy
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
- •ischemic cardiomyopathyI25.5
- •peripartum cardiomyopathyO90.3
- •ventricular hypertrophyI51.7
Code First
The underlying condition must be sequenced before this code
Related Codes(9)
I42.0Dilated cardiomyopathy
I42.1Obstructive hypertrophic cardiomyopathy
I42.2Other hypertrophic cardiomyopathy
I42.3Endomyocardial (eosinophilic) disease
I42.4Endocardial fibroelastosis
I42.5Other restrictive cardiomyopathy
I42.6Alcoholic cardiomyopathy
I42.7Cardiomyopathy due to drug and external agent
I42.9Cardiomyopathy, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(118)
SNOMED CT
- Degeneration of heart64077000
- Mural degeneration of heart64077000
- Muscular degeneration of heart64077000
- Myocardial degeneration64077000
- Nonobstructive cardiomyopathy69609002
- Cardiomyopathy85898001
- Myocardiopathy85898001
- Primary cardiomyopathy89461002
- Cardiomyopathy due to mucopolysaccharidosis195027000
- Mucopolysaccharidosis cardiomyopathy195027000
- Dystrophic cardiomyopathy195032004
- Post-myocarditic cardiomyopathy233875006
- Arrhythmogenic right ventricular cardiomyopathy253528005
- Arrhythmogenic right ventricular dysplasia253528005
- Congenital woolly hair254231002
- Congenital wooly hair254231002
- Autosomal recessive familial woolly hair403795009
- Autosomal recessive familial wooly hair403795009
- Hypertrophy of septomarginal trabeculation406428006
- Moderator band cardiomyopathy406428006
- Right ventricular myocardial noncompaction cardiomyopathy447934002
- Left ventricular myocardial noncompaction cardiomyopathy447935001
- Histiocytoid mitochondrial cardiomyopathy due to cytochrome aa3 deficiency460500001
- Inflammatory cardiomyopathy471841009
- Disorder of heart muscle associated with rejection of cardiac transplant471851005
- Disorder of myocardium associated with rejection of cardiac transplant471851005
- Cardiomyopathy due to disorder of heart valve471858004
- Valvular cardiomyopathy471858004
- Disorder of heart muscle due to sickle cell haemoglobinopathy471863000
- Disorder of heart muscle due to sickle cell hemoglobinopathy471863000
- Disorder of myocardium due to sickle cell haemoglobinopathy471863000
- Disorder of myocardium due to sickle cell hemoglobinopathy471863000
- Ventricular myocardial noncompaction cardiomyopathy471875005
- Mitochondrial cardiomyopathy472315005
- Hypertrophic mitochondrial cardiomyopathy472316006
- Histiocytoid mitochondrial cardiomyopathy472317002
- Hypertrophic mitochondrial cardiomyopathy associated with cataracts and lactic acidosis472318007
- Fatal infantile mitochondrial cardiomyopathy472319004
- Maternally inherited mitochondrial cardiomyopathy and myopathy472320005
- Keratoderma with woolly hair type I715535009
- Keratoderma with wooly hair type I715535009
- Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome715535009
- Naxos disease715535009
- Palmoplantar hyperkeratosis with arrhythmogenic cardiomyopathy715535009
- Familial isolated ARVD (arrhythmogenic right ventricular dysplasia)715865008
- Familial isolated arrhythmogenic right ventricular cardiomyopathy715865008
- Familial isolated arrhythmogenic right ventricular dysplasia715865008
- Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation718212006
- TMEM70 related mitochondrial encephalo-cardio-myopathy718212006
- Coenzyme Q10 deficiency724575009
- Cardiomyopathy due to storage disease860839005
- Infiltrative cardiomyopathy871646007
- Arrhythmogenic left ventricular cardiomyopathy880040003
- Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome1172839002
- COQ4-related neonatal encephalomyopathy1186718008
- Coenzyme Q4-related neonatal encephalomyopathy1186718008
- Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome1186718008
- Maternally inherited mitochondrial cardiomyopathy1187635008
- Macrocephaly, intellectual disability, left ventricular non compaction syndrome1187642008
Clinical Terms
- Arrhythmogenic right ventricular dysplasia
- Myocardial degeneration
- TMEM70 related mitochondrial encephalo-cardio-myopathy
- Myocardiopathy
- Primary cardiomyopathy
- Fatal infantile mitochondrial cardiomyopathy
- Disorder of myocardium associated with rejection of cardiac transplant
- Cardiomyopathy due to disorder of heart valve
- Familial isolated arrhythmogenic right ventricular cardiomyopathy
- Muscular degeneration of heart
- Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome
- Disorder of myocardium due to sickle cell hemoglobinopathy
- Hypertrophic mitochondrial cardiomyopathy
- Mitochondrial cardiomyopathy
- Autosomal recessive familial woolly hair
- Arrhythmogenic right ventricular cardiomyopathy
- Arrhythmogenic left ventricular cardiomyopathy
- Familial isolated ARVD (arrhythmogenic right ventricular dysplasia)
- Left ventricular myocardial noncompaction cardiomyopathy
- Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome
- Hypertrophy of septomarginal trabeculation
- Disorder of heart muscle due to sickle cell haemoglobinopathy
- Maternally inherited mitochondrial cardiomyopathy and myopathy
- Coenzyme Q10 deficiency
- Cardiomyopathy due to mucopolysaccharidosis
- Inflammatory cardiomyopathy
- Mucopolysaccharidosis cardiomyopathy
- Cardiomyopathy due to storage disease
- Right ventricular myocardial noncompaction cardiomyopathy
- Congenital wooly hair
- COQ4-related neonatal encephalomyopathy
- Disorder of myocardium due to sickle cell haemoglobinopathy
- Dystrophic cardiomyopathy
- Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome
- Post-myocarditic cardiomyopathy
- Moderator band cardiomyopathy
- Mural degeneration of heart
- Disorder of heart muscle associated with rejection of cardiac transplant
- Naxos disease
- Autosomal recessive familial wooly hair
- Hypertrophic mitochondrial cardiomyopathy associated with cataracts and lactic acidosis
- Nonobstructive cardiomyopathy
- Degeneration of heart
- Infiltrative cardiomyopathy
- Maternally inherited mitochondrial cardiomyopathy
- Histiocytoid mitochondrial cardiomyopathy
- Valvular cardiomyopathy
- Congenital woolly hair
- Palmoplantar hyperkeratosis with arrhythmogenic cardiomyopathy
- Coenzyme Q4-related neonatal encephalomyopathy
- Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation
- Histiocytoid mitochondrial cardiomyopathy due to cytochrome aa3 deficiency
- Keratoderma with woolly hair type I
- Keratoderma with wooly hair type I
- Ventricular myocardial noncompaction cardiomyopathy
- Familial isolated arrhythmogenic right ventricular dysplasia
- Disorder of heart muscle due to sickle cell hemoglobinopathy
- Macrocephaly, intellectual disability, left ventricular non compaction syndrome
Frequently Asked Questions
What is the ICD-10 code for other cardiomyopathies?
The ICD-10-CM code for other cardiomyopathies is I42.8. The full clinical description is "Other cardiomyopathies". I42.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code I42.8 mean?
ICD-10-CM code I42.8 represents “Other cardiomyopathies”. 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 I42.8 a billable code?
Yes, I42.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is I42.8 in?
I42.8 is in Chapter 9: Diseases of the Circulatory System (codes I00-I99).
What SNOMED CT codes does I42.8 map to?
I42.8 maps to 36 SNOMED CT concepts: 880040003, 253528005, 403795009, 1186718008, 85898001, and 31 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for I42.8?
I42.8 is linked to 1 UMLS Concept Unique Identifier: C0348617. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does I42.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other cardiomyopathies 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 I42.8?
I42.8 maps to the ICD-11 code: BC43.Y (Other specified cardiomyopathy).
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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.