Autosomal Recessive Nonsyndromic Deafness 9
Disease ID: disease_node_14980
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:H90.3, MIM:601071 |
|---|---|
| Subclassof | DOID_0050565 |
| Data Source | DOID |
| Synonyms | DFNB9, NRSD9, autosomal recessive deafness 9, neurosensory nonsyndromic recessive deafness 9 |
| Doid Label | autosomal recessive nonsyndromic deafness 9 |
| Doid Description | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually severe to profound, stable hearing loss and has_material_basis_in mutation in the OTOF gene on chromosome 2p23. |
| Disease Node Id | disease_node_14980 |
| Doid Id | DOID_0110535 |
| Label | Autosomal Recessive Nonsyndromic Deafness 9 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Nonsyndromic Deafness(ID:disease_node_14962) (Disease)