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autosomal recessive nonsyndromic deafness 39
Summary
- Synonym
-
- DFNB39
- autosomal recessive deafness 39
- Definition
- An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21.
- Super Class
- autosomal recessive nonsyndromic deafness
External Links
- Disease Ontology
- DOID:0110497
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P14210 | Hepatocyte growth factor |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q08048 | Hepatocyte growth factor |
