Disease association ontology term - MONDO:0012091 - autosomal recessive nonsyndromic hearing loss 32
Term summary
- ID
- MONDO:0012091
- Name
- autosomal recessive nonsyndromic hearing loss 32
- Ontology or CV name
- Disease association
- Definition
- An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in variation in the chromosome region 1p22.1-p13.3.
