Cochlear nerve aplasia

3 condition reports read genes linked to this trait

Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.

• Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesGREB1LAbout this report →
• Hearing Loss and DeafnessReads 1 of these genesGREB1LAbout this report →
• Congenital Disorders of GlycosylationReads 1 of these genesDHRSXAbout this report →

Every condition report

2 genes linked to Cochlear nerve aplasia

Changes in these genes cause rare conditions in which Cochlear nerve aplasia is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.

How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.

Broader traits

Where this comes from

• The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
• Data release 2026.10.19-9814e911.