autosomal dominant nonsyndromic hearing loss 9
Findings
No curated finding names autosomal dominant nonsyndromic hearing loss 9 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the COCH gene.
Definition from the Mondo Disease Ontology (MONDO:0011058), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Progressive · Young adult onset
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.
- Postlingual sensorineural hearing impairmentHPOHP:0008596
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- COCHHGNC:2180
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2022