Autosomal Domit Nonsyndromic Deafness 20
Disease ID: disease_node_15106
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| Dbxref | ICD10CM:H90.3, MIM:604717 |
|---|---|
| Subclassof | DOID_0050564 |
| Data Source | DOID |
| Synonyms | DFNA20, DFNA26, autosomal dominant deafness 20 |
| Doid Label | autosomal domit nonsyndromic deafness 20 |
| Doid Description | An autosomal domit nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the ACTG1 gene on chromosome 17q25. |
| Disease Node Id | disease_node_15106 |
| Doid Id | DOID_0110550 |
| Label | Autosomal Domit Nonsyndromic Deafness 20 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Nonsyndromic Deafness(ID:disease_node_15056) (Disease)