Autosomal Domit Nonsyndromic Deafness 80
Disease ID: disease_node_15130
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| Dbxref | MIM:619274 |
|---|---|
| Subclassof | DOID_0050564 |
| Data Source | DOID |
| Synonyms | DFNA80, autosomal dominant deafness 80 |
| Doid Label | autosomal domit nonsyndromic deafness 80 |
| Doid Description | An autosomal domit nonsyndromic deafness characterized by congenital deafness associated with absent or malformed cochleae and eighth cranial nerves that has_material_basis_in heterozygous mutation in the GREB1L gene on chromosome 18q11. |
| Disease Node Id | disease_node_15130 |
| Doid Id | DOID_0070602 |
| Label | Autosomal Domit Nonsyndromic Deafness 80 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Nonsyndromic Deafness(ID:disease_node_15056) (Disease)