WormBase Tree Display for DO_term: DOID:0110550
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| DOID:0110550 | Name | autosomal dominant nonsyndromic deafness 20 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the ACTG1 gene on chromosome 17q25. | ||||
| Synonym | Exact | DFNA20 | |||
| DFNA26 | |||||
| autosomal dominant deafness 20 | |||||
| Parent | Is_a | DOID:0050564 | |||
| DB_info | Database | OMIM | disease | 604717 | |
| Attribute_of | Gene_by_orthology | WBGene00000063 | |||
| WBGene00000064 | |||||
| WBGene00000065 | |||||
| WBGene00000066 |
