Disease association ontology term - MONDO:0014237 - autosomal recessive nonsyndromic hearing loss 76
Term summary
- ID
- MONDO:0014237
- Name
- autosomal recessive nonsyndromic hearing loss 76
- Ontology or CV name
- Disease association
- Definition
- Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the SYNE4 gene.
