Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3703346014 | Distal monosomy 12p | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3703347017 | Distal deletion 12p | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3703348010 | Distal monosomy 12p (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3703349019 | 12p13.33 microdeletion syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3703350019 | A rare partial autosomal monosomy with characteristics of language development delay with childhood apraxia of speech, mild intellectual disability, autistic spectrum disorder, attention deficit hyperactivity disorder, anxiety and mildly dysmorphic nonspecific features. Additional clinical features may include muscular hypotonia and joint laxity, hernia and microcephaly. | 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