MYH3 - Gene browser

MYH3

myosin heavy chain 3

HCNC Approved Symbol: MYH3 (HGNC:7573)
Genomic Coordinates: 17:10,628,532 - 10,678,417 (17p13.1)
Synonyms: MYHC-EMB, MYHSE1, HEMHC, SMHCE
Disease Associations: This gene is associated with the following 4 diseases in OMIM.

8Patients

In total, 8 patients were diagnosed with a variant in the MYH3 gene.

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

08
Patient count

Short stature: 3 (37.5%)
Patient Count: 3 (37.5%)
% of total patients presenting each phenotype is shown in parentheses.
3 (37.5%)
Low-set ears: 3 (37.5%)
Patient Count: 3 (37.5%)
% of total patients presenting each phenotype is shown in parentheses.
3 (37.5%)
Multiple pterygia: 3 (37.5%)
Patient Count: 3 (37.5%)
% of total patients presenting each phenotype is shown in parentheses.
3 (37.5%)
Webbed neck: 3 (37.5%)
Patient Count: 3 (37.5%)
% of total patients presenting each phenotype is shown in parentheses.
3 (37.5%)
Scoliosis: 2 (25.0%)
Patient Count: 2 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (25.0%)