OTOA - Gene browser

OTOA

otoancorin

HCNC Approved Symbol: OTOA (HGNC:16378)
Genomic Coordinates: 16:21,663,968 - 21,760,729 (16p12.2)
Synonyms: CT108, DFNB22
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

16Patients

In total, 16 patients were diagnosed with a variant in the OTOA gene.

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

016
Patient count

Hearing loss: 12 (75.0%)
Patient Count: 12 (75.0%)
% of total patients presenting each phenotype is shown in parentheses.
12 (75.0%)
Otitis media: 2 (12.5%)
Patient Count: 2 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
2 (12.5%)
Hearing impairment: 2 (12.5%)
Patient Count: 2 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
2 (12.5%)
Cleft palate: 1 (6.3%)
Patient Count: 1 (6.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (6.3%)
Abnormality of the auditory canal: 1 (6.3%)
Patient Count: 1 (6.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (6.3%)