Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1720751000168115 | Microcephaly, intellectual disability and distinct features, with or without Hirschsprung disease | en | Synonym | Active | Initial character case insensitive | SNOMED Clinical Terms Australian extension |
3008947016 | Mowat-Wilson syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
3009119013 | Mowat-Wilson syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3009165011 | Hirschsprung disease-mental retardation syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3643142016 | Hirschsprung disease-intellectual disability syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Mowat-Wilson syndrome due to monosomy 2q22 | Is a | True | Mowat-Wilson syndrome | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set