HCM - Hypertrophic non-obstructive cardiomyopathy
Nonobstructive hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy due to neuromuscular disorder
Hypertrophic cardiomyopathy without obstruction (disorder)
Hypertrophic cardiomyopathy of apex of heart
LVA - Left ventricular aneurysm
Hypertrophic cardiomyopathy due to glycogen storage disease
Hypertrophic cardiomyopathy
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
Hypertrophic cardiomyopathy with genetic marker
Hypertrophic mitochondrial cardiomyopathy
Combined oxidative phosphorylation defect type 16
Hypertrophic cardiomyopathy due to disorder
Apical hypertrophic cardiomyopathy with aneurysm
Primary hypertrophic cardiomyopathy
Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease
COXPD10 - combined oxidative phosphorylation defect type 10
Hypertrophic cardiomyopathy due to hyperthyroidism
Left ventricular wall aneurysmal
Primary familial cardiomyopathy
Hypertrophic non-obstructive cardiomyopathy
Progressive sensorineural deafness and hypertrophic cardiomyopathy syndrome
Combined oxidative phosphorylation defect type 10
Familial cardiomyopathy
Cardiomyopathy due to storage disease
Aneurysm of apex of heart due to apical hypertrophic cardiomyopathy
LV wall aneurysmal
Left ventricular aneurysm
Lysosomal disease with hypertrophic cardiomyopathy
Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome
Hypertrophic cardiomyopathy due to Friedreich ataxia
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation
Primary familial hypertrophic cardiomyopathy
Primary idiopathic hypertrophic cardiomyopathy
Fatal congenital hypertrophic cardiomyopathy due to glycogenosis
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimisation 1 deficiency
Apical hypertrophic cardiomyopathy
Glycogen storage disease with hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation
Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency
Hypertrophic mitochondrial cardiomyopathy associated with cataracts and lactic acidosis
Hypertrophic cardiomyopathy due to lysosomal disease
Cardiomyopathy in Friedreich ataxia
Hypertrophic cardiomyopathy without obstruction
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimization 1 deficiency
HCM - Hypertrophic cardiomyopathy
Cardiomyopathy in Friedreich's ataxia

Frequently Asked Questions

What is the ICD-10 code for other hypertrophic cardiomyopathy?

The ICD-10-CM code for other hypertrophic cardiomyopathy is I42.2. The full clinical description is "Other hypertrophic cardiomyopathy". I42.2 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code I42.2 mean?

ICD-10-CM code I42.2 represents “Other hypertrophic cardiomyopathy”. 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 I42.2 a billable code?

Yes, I42.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is I42.2 in?

I42.2 is in Chapter 9: Diseases of the Circulatory System (codes I00-I99).

What SNOMED CT codes does I42.2 map to?

I42.2 maps to 26 SNOMED CT concepts: 1204192000, 1204194004, 771478008, 860839005, 195030007, and 21 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for I42.2?

I42.2 is linked to 2 UMLS Concept Unique Identifiers: C0340425, C0348615. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does I42.2 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other hypertrophic cardiomyopathy 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 I42.2?

I42.2 maps to the ICD-11 code: BC43.1Z (Hypertrophic 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.