MYO15A - Gene browser

MYO15A

myosin XVA

HCNC Approved Symbol: MYO15A (HGNC:7594)
Genomic Coordinates: 17:18,108,756 - 18,179,800 (17p11.2)
Synonyms: DFNB3, MYO15
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

101Patients

In total, 101 patients were diagnosed with a variant in the MYO15A gene.

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

0101
Patient count

Hearing loss: 39 (38.6%)
Patient Count: 39 (38.6%)
% of total patients presenting each phenotype is shown in parentheses.
39 (38.6%)
Hearing impairment: 20 (19.8%)
Patient Count: 20 (19.8%)
% of total patients presenting each phenotype is shown in parentheses.
20 (19.8%)
Deafness: 9 (8.9%)
Patient Count: 9 (8.9%)
% of total patients presenting each phenotype is shown in parentheses.
9 (8.9%)
Congenital deafness: 9 (8.9%)
Patient Count: 9 (8.9%)
% of total patients presenting each phenotype is shown in parentheses.
9 (8.9%)
Intellectual disability: 8 (7.9%)
Patient Count: 8 (7.9%)
% of total patients presenting each phenotype is shown in parentheses.
8 (7.9%)