Disease association ontology term - MONDO:0010986 - autosomal recessive nonsyndromic hearing loss 9
Term summary
- ID
- MONDO:0010986
- Name
- autosomal recessive nonsyndromic hearing loss 9
- Ontology or CV name
- Disease association
- Definition
- Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the OTOF gene.
