Autosomal Recessive Nonsyndromic Deafness 3
Disease ID: disease_node_15027
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| Dbxref | ICD10CM:H90.3, MIM:600316 |
|---|---|
| Subclassof | DOID_0050565 |
| Data Source | DOID |
| Synonyms | DFNB3, NRSD3, autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3 |
| Doid Label | autosomal recessive nonsyndromic deafness 3 |
| 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 MYO15A gene on chromosome 17p11. |
| Disease Node Id | disease_node_15027 |
| Doid Id | DOID_0110488 |
| Label | Autosomal Recessive Nonsyndromic Deafness 3 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Nonsyndromic Deafness(ID:disease_node_14962) (Disease)