2015 ICD-9-CM Diagnosis Code 425.4
Other primary cardiomyopathies
- 2015
- Billable Thru Sept 30/2015
- Non-Billable On/After Oct 1/2015
- ICD-9-CM 425.4 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 425.4 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
Convert to ICD-10-CM:
425.4 converts approximately to:
- 2015/16 ICD-10-CM I42.5 Other restrictive cardiomyopathy
Or:
- 2015/16 ICD-10-CM I42.8 Other cardiomyopathies
Approximate Synonyms
- Arrhythmogenic right ventricular cardiomyopathy
- Benign scapuloperoneal muscular dystrophy with cardiomyopathy
- Cardiomyopathy
- Cardiomyopathy (disease of heart muscle)
- Cardiomyopathy associated with another disorder
- Cardiomyopathy dilated
- Cardiomyopathy, dilated
- Cardiomyopathy, dilated, nonischemic
- Cardiomyopathy, idiopathic
- Cardiomyopathy, primary
- Cardiomyopathy, primary (heart condition)
- Cardiomyopathy, restrictive
- CHF w cardiomyopathy
- Congestive cardiomyopathy
- Congestive heart failure (chf) with cardiomyopathy
- Congestive heart failure due to cardiomyopathy
- Congestive obstructive cardiomyopathy
- Dilated cardiomyopathy
- Dystrophic cardiomyopathy
- Endomyocardial disease
- Familial cardiomyopathy
- Familial restrictive cardiomyopathy
- Fixed myocardial perfusion defect
- Hypertrophic cardiomyopathy
- Hypertrophic cardiomyopathy without obstruction
- Idiopathic cardiomyopathy
- Left ventricular noncompaction
- Myocardial perfusion defect
- Nonischemic congestive cardiomyopathy
- Nonischemic dilated cardiomyopathy
- Nonischemic dilated cardiomyopathy (heart condition)
- Nonobstructive cardiomyopathy
- Partially reversible myocardial perfusion defect
- Primary cardiomyopathy
- Primary dilated cardiomyopathy
- Primary endomyocardial fibrosis restrictive cardiomyopathy
- Primary eosinophilic endomyocardial cardiomyopathy
- Primary eosinophilic endomyocardial restrictive cardiomyopathy
- Primary familial dilated cardiomyopathy
- Primary familial hypertrophic cardiomyopathy
- Primary idiopathic dilated cardiomyopathy
- Primary idiopathic hypertrophic cardiomyopathy
- Primary idiopathic restrictive cardiomyopathy
- Primary restrictive cardiomyopathy
- Restrictive cardiomyopathy
- Restrictive cardiomyopathy (heart condition)
- Restrictive cardiomyopathy secondary to familial storage disease
- Restrictive cardiomyopathy secondary to glycogen storage disease
- Restrictive cardiomyopathy with endomyocardial fibrosis
- Restrictive cardiomyopathy without endomyocardial fibrosis
- Reversible myocardial perfusion defect
- Secondary restrictive cardiomyopathy
- Specific heart muscle disorder
- Tachycardia-induced cardiomyopathy
Clinical Information
- A condition in which the myocardium is hypertrophied without an obvious cause. The hypertrophy is generally asymmetric and may be associated with obstruction of the ventricular outflow tract
- A disease of the heart muscle or myocardium proper whose cause is unknown
- A disease of the heart muscle or myocardium proper. Cardiomyopathies may be classified as either primary or secondary, on the basis of etiology, or on the pathophysiology of the lesion: hypertrophic, dilated, or restrictive
- Condition in which there is a deviation from or interruption of the normal structure or function of the myocardium, the middle and thickest layer of the heart wall, composed of heart muscle
- Myocardial disease characterized by hypertrophy, involving mainly the interventricular septum, interfering with left ventricular emptying
Applies To
- Cardiomyopathy:
- NOS
- congestive
- constrictive
- familial
- idiopathic
- obstructive
- restrictive
- Cardiovascular collagenosis
idiopathic 425.4
alcoholic 425.5
