Currently, this gene is not associated with any human disease in OMIM. However, the following publication(s) suggest a possible gene disease association.
Diagnosed Cases
8Patients
In total, 8 patients were diagnosed with a variant in the MYH7B gene.
Frequently observed phenotypes(Top 5 only)
(Top 5 only, Patient count*) *% of total patients presenting each phenotype is shown in parentheses.
08 Patient count
Left ventricular hypertrophy
8 (100.0%)
Patient Count: 8 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
8 (100.0%)
Hypertrophic cardiomyopathy
1 (12.5%)
Patient Count: 1 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
1 (12.5%)
Palpitations
1 (12.5%)
Patient Count: 1 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
1 (12.5%)
Presyncope
1 (12.5%)
Patient Count: 1 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
1 (12.5%)
Right ventricular hypertrophy
1 (12.5%)
Patient Count: 1 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
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