Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
353381016 | Congenital microvillous atrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
353382011 | Davidson disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
624225011 | Congenital microvillous atrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Familial absence of villi | Is a | True | Congenital microvillous atrophy | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set