Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1221474011 | Deletion of short arm of chromosome 4 | en | Synonym | Active | Case insensitive | SNOMED CT core |
28958010 | 4p partial monosomy syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
28959019 | Chromosome 4 short arm deletion syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
28960012 | 4p minus syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
28961011 | Midline fusion defect syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
744279014 | 4p partial monosomy syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn) | Is a | False | 4p partial monosomy syndrome | Inferred relationship | Some | |
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn) | Associated with | True | 4p partial monosomy syndrome | Inferred relationship | Some | 2 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set