WormBase Tree Display for DO_term: DOID:0111274
expand all nodes | collapse all nodes | view schema
| DOID:0111274 | Name | CODAS syndrome | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A syndrome characterized by developmental delay, and cerebral, ocular, dental, auricular, and skeletal anomalies that has_material_basis_in homozygous or compound heterozygous mutation in LONP1 on 19p13.3. | ||||
| Synonym | Exact | cerebral, ocular, dental, auricular, and skeletal syndrome | |||
| cerebro-oculo-dento-auriculo-skeletal syndrome | |||||
| Parent | Is_a | DOID:225 | |||
| DOID:0050737 | |||||
| DB_info | Database | OMIM | disease | 600373 | |
| Attribute_of | Gene_by_orthology | WBGene00016391 |
