Autosomal Domit Nonsyndromic Deafness 2B
Disease ID: disease_node_15097
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:H90.3, MIM:612644 |
|---|---|
| Subclassof | DOID_0050564 |
| Data Source | DOID |
| Synonyms | DFNA2B, autosomal dominant deafness 2B |
| Doid Label | autosomal domit nonsyndromic deafness 2B |
| Doid Description | An autosomal domit nonsyndromic deafness that is characterized postlingual onset in the fourth decade of life with by high frequency progressive hearing loss and has_material_basis_in mutation in the GJB3 gene on chromosome 1p34.3. |
| Disease Node Id | disease_node_15097 |
| Doid Id | DOID_0110559 |
| Label | Autosomal Domit Nonsyndromic Deafness 2B |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Nonsyndromic Deafness(ID:disease_node_15056) (Disease)