MYH7 - Gene browser

MYH7

myosin heavy chain 7

HCNC Approved Symbol: MYH7 (HGNC:7577)
Genomic Coordinates: 14:23,412,740 - 23,435,660 (14q11.2)
Synonyms: CMD1S, CMH1, MPD1
Disease Associations: This gene is associated with the following 6 diseases in OMIM.

Diagnosed Cases

271Patients

In total, 271 patients were diagnosed with a variant in the MYH7 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

0271
Patient count

Left ventricular hypertrophy: 183 (67.5%)
Patient Count: 183 (67.5%)
% of total patients presenting each phenotype is shown in parentheses.
183 (67.5%)
Heart failure: 51 (18.8%)
Patient Count: 51 (18.8%)
% of total patients presenting each phenotype is shown in parentheses.
51 (18.8%)
Arrhythmias: 41 (15.1%)
Patient Count: 41 (15.1%)
% of total patients presenting each phenotype is shown in parentheses.
41 (15.1%)
Hypertrophic cardiomyopathy: 28 (10.3%)
Patient Count: 28 (10.3%)
% of total patients presenting each phenotype is shown in parentheses.
28 (10.3%)
Heart conduction disorder: 16 (5.9%)
Patient Count: 16 (5.9%)
% of total patients presenting each phenotype is shown in parentheses.
16 (5.9%)