Autosomal Domit Nonsyndromic Deafness 15
Disease ID: disease_node_15110
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| Dbxref | ICD10CM:H90.3, MIM:602459 |
|---|---|
| Subclassof | DOID_0050564 |
| Data Source | DOID |
| Synonyms | DFNA15, DFNA52, autosomal dominant deafness 15, autosomal dominant deafness 52, autosomal dominant nonsyndromic deafness 52 |
| Doid Label | autosomal domit nonsyndromic deafness 15 |
| 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 POU4F3 gene on chromosome 5q32. |
| Disease Node Id | disease_node_15110 |
| Doid Id | DOID_0110546 |
| Label | Autosomal Domit Nonsyndromic Deafness 15 |
| Doid Alternate Ids | DOID_0110578 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Nonsyndromic Deafness(ID:disease_node_15056) (Disease)