Autosomal Domit Nonsyndromic Deafness 25
Disease ID: disease_node_15101
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| Dbxref | ICD10CM:H90.3, MIM:605583 |
|---|---|
| Subclassof | DOID_0050564 |
| Data Source | DOID |
| Synonyms | DFNA25, autosomal dominant deafness 25 |
| Doid Label | autosomal domit nonsyndromic deafness 25 |
| Doid Description | An autosomal domit 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. |
| Disease Node Id | disease_node_15101 |
| Doid Id | DOID_0110555 |
| Label | Autosomal Domit Nonsyndromic Deafness 25 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Nonsyndromic Deafness(ID:disease_node_15056) (Disease)