WormBase Tree Display for DO_term: DOID:0110826
expand all nodes | collapse all nodes | view schema
| DOID:0110826 | Name | Usher syndrome type 1 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | An Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa. | ||||
| Synonym | Exact | US1 | |||
| USH1 | |||||
| Parent | Is_a | DOID:0050439 | |||
| Child | Is | DOID:0110830 | |||
| DOID:0110831 | |||||
| DOID:0110832 | |||||
| DOID:0110833 | |||||
| DOID:0110834 | |||||
| DOID:0110835 | |||||
| DOID:0110836 | |||||
| DOID:0110837 | |||||
| DB_info | Database | OMIM | disease | 276900 | |
| Attribute_of | Gene_by_orthology | WBGene00002039 |
