Autosomal Domit Nonsyndromic Deafness 28
Disease ID: disease_node_15099
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| Dbxref | ICD10CM:H90.3, MIM:608641 |
|---|---|
| Subclassof | DOID_0050564 |
| Data Source | DOID |
| Synonyms | DFNA28, autosomal dominant deafness 28 |
| Doid Label | autosomal domit nonsyndromic deafness 28 |
| Doid Description | An autosomal domit nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the GRHL2 gene on chromosome 8q22. |
| Disease Node Id | disease_node_15099 |
| Doid Id | DOID_0110557 |
| Label | Autosomal Domit Nonsyndromic Deafness 28 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Nonsyndromic Deafness(ID:disease_node_15056) (Disease)