Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
10975019 | 10p partial monosomy syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
798927012 | 10p partial monosomy syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion | Is a | True | 10p partial monosomy syndrome | Inferred relationship | Some | |
Distal monosomy 10p | Is a | True | 10p partial monosomy syndrome | Inferred relationship | Some | |
Hypoparathyroidism, deafness, renal disease syndrome | Is a | True | 10p partial monosomy syndrome | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set