Disease association ontology term - MONDO:0013386 - autosomal recessive nonsyndromic hearing loss 74
Term summary
- ID
- MONDO:0013386
- Name
- autosomal recessive nonsyndromic hearing loss 74
- Ontology or CV name
- Disease association
- Definition
- Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MSRB3 gene.
