autosomal dominant nonsyndromic hearing loss 47
MONDO:0012090Mondo
Findings
No curated finding names autosomal dominant nonsyndromic hearing loss 47 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 9p22-p21.
Definition from the Mondo Disease Ontology (MONDO:0012090), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
1 feature
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