GénOncoPGxBio
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COCH

HGNC ↗

Autosomal dominant non-syndromic sensorineural hearing loss (DFNA9)

1 article(s) in the watch · Constitutional genetics

Curated publications

6/10

COCH-Related Hearing Loss in a French Cohort: Novel Variants and Genotype–Phenotype Correlations

Autosomal dominant non-syndromic sensorineural hearing loss (DFNA9)

Gén.20 May 2026

External references

OMIM ↗GeneReviews ↗ClinVar ↗NCBI Gene ↗

Automatic aggregation page — a clinical introduction may be added.