Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3643466016 | Sporadic foetal brain disruption sequence | en | Synonym | Active | Case insensitive | SNOMED CT core |
3643467013 | Sporadic fetal brain disruption sequence | en | Synonym | Active | Case insensitive | SNOMED CT core |
3643469011 | Sporadic fetal brain disruption sequence (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3643468015 | A rare non-syndromic central nervous system malformation disorder with characteristics of severe microcephaly, overlapping sutures, keel-like occipital bone prominence, scalp rugae with normal hair pattern and signs of neurological impairment. Brain imaging may show ventriculomegaly, cortical tissue deficit, and hydranencephaly. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set