Disease association ontology term - MONDO:0013471 - autosomal recessive nonsyndromic hearing loss 61
Term summary
- ID
- MONDO:0013471
- Name
- autosomal recessive nonsyndromic hearing loss 61
- Ontology or CV name
- Disease association
- Definition
- Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the SLC26A5 gene.
