Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
136345015 | Treacher Collins syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
136346019 | Mandibulofacial dysostosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3788353018 | Franceschetti Klein syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
823577011 | Treacher Collins syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
3788354012 | A congenital disorder of craniofacial development with characteristics of bilateral symmetrical oto-mandibular dysplasia without abnormalities of the extremities, and associated with several head and neck defects. The syndrome is caused by mutations in the TCOF1 gene (5q32) encoding the nucleolar phosphoprotein Treacle or in the POLR1C (6p21.1) or POLR1D (13q12.2) genes, coding for RNA polymerase I and III subunits. Transmission is autosomal dominant with 90% penetrance and variable expressivity, even among affected patients within the same family. Mutations in POLR1C gene are inherited in autosomal recessive manner. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Franceschetti-Klein syndrome | Is a | False | Treacher Collins syndrome | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set