|
| General Information | |||
|---|---|---|---|
| Term | autosomal dominant nonsyndromic deafness 80 | ID (Ontology) | DOID:0070602 (Human Disease) |
| Definition | An autosomal dominant 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. | ||
| Also Known As | "autosomal dominant deafness 80" ; "DFNA80" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
nonsyndromic deafness_______ autosomal dominant disease__| autosomal dominant nonsyndromic deafness |__autosomal dominant nonsyndromic deafness 80 |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | autosomal dominant nonsyndromic deafness | ||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
| MIM:619274 | |||