Disease association ontology term - MONDO:0011350 - autosomal dominant nonsyndromic hearing loss 17
Term summary
- ID
- MONDO:0011350
- Name
- autosomal dominant nonsyndromic hearing loss 17
- Ontology or CV name
- Disease association
- Definition
- Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH9 gene.
