Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3644656013 | Oro-facial digital syndrome type 12 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3644657016 | Orofaciodigital syndrome type 12 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3644658014 | Oro-facial digital syndrome type 12 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3644659018 | Moran Barroso syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3664244011 | A rare subtype of orofaciodigital syndrome with sporadic occurrence and characteristics of cardiac (septum hypertrophy) and central nervous system abnormalities (myelomeningocele, Sylvius aqueduct stenosis, corpus callosum agenesis, vermis hypoplasia), in addition to oral, facial and digital malformations (gingival frenulum, bifid tongue, supernumerary teeth, macrocephaly, hypertelorism, pre- and post-axial polydactyly in hands, preaxial polydactyly in feet and club feet). Skeletal anomalies, such as short tibiae and central, Y-shaped metacarpals are also associated. | 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
Cardiovascular finding reference set
Problem/Diagnosis reference set