Disease association ontology term - MONDO:0011568 - autosomal dominant nonsyndromic hearing loss 25
Term summary
- ID
- MONDO:0011568
- Name
- autosomal dominant nonsyndromic hearing loss 25
- Ontology or CV name
- Disease association
- Definition
- Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the SLC17A8 gene.
