Autosomal Recessive Nonsyndromic Deafness 61
Disease ID: disease_node_15002
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:H90.3, MIM:613865 |
|---|---|
| Subclassof | DOID_0050565 |
| Data Source | DOID |
| Synonyms | DFNB61, autosomal recessive deafness 61 |
| Doid Label | autosomal recessive nonsyndromic deafness 61 |
| Doid Description | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the SLC26A5 gene on chromosome 7q22. |
| Disease Node Id | disease_node_15002 |
| Doid Id | DOID_0110513 |
| Label | Autosomal Recessive Nonsyndromic Deafness 61 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Nonsyndromic Deafness(ID:disease_node_14962) (Disease)