Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3757572012 | Stickler syndrome non-ocular type | en | Synonym | Active | Case sensitive | SNOMED CT core |
3757573019 | Stickler syndrome type 3 (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
3757574013 | Stickler syndrome type 3 | en | Synonym | Active | Case sensitive | SNOMED CT core |
4945009011 | Autosomal dominant otospondylomegaepiphyseal dysplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
4945010018 | AD OSMED - autosomal dominant otospondylomegaepiphyseal dysplasia | en | Synonym | Active | Case sensitive | SNOMED CT core |
3757575014 | A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of craniofacial dysmorphism (midface hypoplasia, depressed nasal bridge, small nose with upturned tip, cleft palate, Pierre Robin sequence), bilateral, pronounced sensorineural hearing loss and skeletal/joint anomalies (including spondyloepiphyseal dysplasia, arthralgia/arthropathy), in the absence of ocular abnormalities. There is evidence the disease is caused by heterozygous mutation in the COL11A2 gene on chromosome 6p21. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set