Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3726043010 | Deafness with onychodystrophy syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3726044016 | Deafness with onychodystrophy syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3726045015 | A group of rare genetic developmental defect during embryogenesis disorders with the association of sensorineural deafness and onychodystrophy (for example absent/hypoplastic finger and toenails) as well as brachydactyly and finger-like thumbs. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
DOORS syndrome | Is a | True | Deafness with onychodystrophy syndrome | Inferred relationship | Some | |
Autosomal dominant deafness with onychodystrophy syndrome | Is a | True | Deafness with onychodystrophy syndrome | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set