Autosomal Domit Nonsyndromic Deafness 2A
Disease ID: disease_node_15098
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:H90.3, MIM:600101 |
|---|---|
| Subclassof | DOID_0050564 |
| Data Source | DOID |
| Synonyms | DFNA2A, autosomal dominant deafness 2A |
| Doid Label | autosomal domit nonsyndromic deafness 2A |
| Doid Description | An autosomal domit nonsyndromic deafness that is characterized by high frequency progressive hearing loss and has_material_basis_in mutation in the KCNQ4 gene on chromosome 1p34.2. |
| Disease Node Id | disease_node_15098 |
| Doid Id | DOID_0110558 |
| Label | Autosomal Domit Nonsyndromic Deafness 2A |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Nonsyndromic Deafness(ID:disease_node_15056) (Disease)