WormBase Tree Display for DO_term: DOID:0110541
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| DOID:0110541 | Name | autosomal dominant nonsyndromic deafness 1 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | An autosomal dominant nonsyndromic deafness that is characterized by low frequency progressive hearing loss and has_material_basis_in mutation in the DIAPH1 gene on chromosome 5q31. | ||||
| Synonym | Exact | DFNA1 | |||
| Konigsmark syndrome | |||||
| LFHL1 | |||||
| autosomal dominant deafness 1 | |||||
| autosomal dominant deafness 1, with or without thrombocytopenia | |||||
| hereditary low frequency hearing loss 1 | |||||
| Parent | Is_a | DOID:0050564 | |||
| DB_info | Database | OMIM | disease | 124900 | |
| Attribute_of | Gene_by_orthology | WBGene00000872 |
