Hypertrophic cardiomyopathy 2

Hypertrophic cardiomyopathy 2

Definition

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene.

Also known as cardiomyopathy, familial hypertrophic, type 2, cardiomyopathy, hypertrophic, 2, CMH2, familial hypertrophic cardiomyopathy type 2, hypertrophic cardiomyopathy 2, hypertrophic cardiomyopathy caused by mutation in TNNT2, hypertrophic cardiomyopathy type 2, TNNT2 hypertrophic cardiomyopathy — per MONDO

Also identified as

Affected Organs

Organ Involvement Source
Cardiovascular system Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Cardiovascular system Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Heart Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Heart Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Musculature Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Musculature Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Musculoskeletal system Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Musculoskeletal system Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Myocardium Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Respiratory system Disease Has Associated Anatomic Site NCIT · CC BY 4.0