Autosomal Recessive Nonsyndromic Deafness 6
Disease ID: disease_node_15003
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:H90.3, MIM:600971 |
|---|---|
| Subclassof | DOID_0050565 |
| Data Source | DOID |
| Synonyms | DFNB6, autosomal recessive deafness 6 |
| Doid Label | autosomal recessive nonsyndromic deafness 6 |
| 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 TMIE gene on chromosome 3p21. |
| Disease Node Id | disease_node_15003 |
| Doid Id | DOID_0110512 |
| Label | Autosomal Recessive Nonsyndromic Deafness 6 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Nonsyndromic Deafness(ID:disease_node_14962) (Disease)