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autosomal dominant nonsyndromic deafness 25
Summary
- Synonym
-
- DFNA25
- autosomal dominant deafness 25
- Definition
- An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second-sixth decade of life with high frequency progressive hearing loss and has_material_basis_in mutation in the SLC17A8 gene on chromosome 12q23.
- Super Class
- autosomal dominant nonsyndromic deafness
External Links
- Disease Ontology
- DOID:0110555
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q8NDX2 | Vesicular glutamate transporter 3 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q3TYG5 | Ion transport domain-containing protein | |
| Q8BFU8 | Vesicular glutamate transporter 3 |
