Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4572065017 | Y disomy | en | Synonym | Active | Case sensitive | SNOMED CT core |
4572066016 | 47,XYY syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
788571019 | Double Y syndrome (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
84580015 | Double Y syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
84581016 | XYY syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
4572067013 | A sex chromosome aneuploidy where males receive an additional Y chromosome, and with clinical characteristics of tall stature evident from childhood, macrocephaly, facial features (mild hypertelorism, low set ears, a mildly flat malar region), speech delay and an increased risk for social and emotional difficulties, attention deficit hyperactive disorder and autistic spectrum disorder. | 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
Problem/Diagnosis reference set