Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3323103015 | Epiphyseal dysplasia, microcephalus, nystagmus syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3323104014 | Epiphyseal dysplasia, microcephalus, nystagmus syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3323105010 | Lowry Wood syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3323106011 | Syndrome with the association of epiphyseal dysplasia, short stature, microcephaly and in the first reported cases congenital nystagmus. So far, less than 10 cases have been described in the literature. Variable degrees of intellectual deficit have also been reported. Other occasional features include retinitis pigmentosa and coxa vara. Transmission appears to be autosomal recessive. | 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