Status: current, Defined. Date: 31-Jul 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
787130016 | Microgyria (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
9257015 | Microgyria | en | Synonym | Active | Case insensitive | SNOMED CT core |
9258013 | Polymicrogyria | en | Synonym | Active | Case insensitive | SNOMED CT core |
9259017 | Micropolygyria | en | Synonym | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Microcephaly, polymicrogyria, corpus callosum agenesis syndrome | Is a | True | Microgyria | Inferred relationship | Some | |
Occipital pachygyria and polymicrogyria | Is a | True | Microgyria | Inferred relationship | Some | |
Congenital bilateral perisylvian syndrome | Is a | False | Microgyria | Inferred relationship | Some | |
Unilateral polymicrogyria | Is a | True | Microgyria | Inferred relationship | Some | |
Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome | Is a | True | Microgyria | Inferred relationship | Some | |
Bilateral polymicrogyria | Is a | True | Microgyria | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set