Autosomal Recessive Nonsyndromic Deafness 39
Disease ID: disease_node_15018
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| Dbxref | ICD10CM:H90.3, MIM:608265 |
|---|---|
| Subclassof | DOID_0050565 |
| Data Source | DOID |
| Synonyms | DFNB39, autosomal recessive deafness 39 |
| Doid Label | autosomal recessive nonsyndromic deafness 39 |
| Doid Description | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21. |
| Disease Node Id | disease_node_15018 |
| Doid Id | DOID_0110497 |
| Label | Autosomal Recessive Nonsyndromic Deafness 39 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Nonsyndromic Deafness(ID:disease_node_14962) (Disease)