MYH11 - Gene browser

MYH11

myosin heavy chain 11

HCNC Approved Symbol: MYH11 (HGNC:7569)
Genomic Coordinates: 16:15,703,135 - 15,857,028 (16p13.11)
Synonyms: SMMHC, SMHC, SMMS-1
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

10Patients

In total, 10 patients were diagnosed with a variant in the MYH11 gene.

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

010
Patient count

Aortic aneurysm: 2 (20.0%)
Patient Count: 2 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (20.0%)
Pectus excavatum: 2 (20.0%)
Patient Count: 2 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (20.0%)
Abdominal distension: 1 (10.0%)
Patient Count: 1 (10.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (10.0%)
Facial dysmorphism: 1 (10.0%)
Patient Count: 1 (10.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (10.0%)
Hydroureter: 1 (10.0%)
Patient Count: 1 (10.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (10.0%)