autosomal dominant nonsyndromic hearing loss 53
MONDO:0012380Mondo
Findings
No curated finding names autosomal dominant nonsyndromic hearing loss 53 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 14q11.2-q12.
Definition from the Mondo Disease Ontology (MONDO:0012380), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Juvenile onset · Early young adult onset
HPO, annotations 2026-09-02
Features
2 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Sensorineural hearing impairmentHPOHP:0000407
- 16 of 16 reported patients · Juvenile onset
- Abnormal vestibular functionHPOHP:0001751
- 0 of 6 reported patients