Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3737487011 | Primary non-essential cutis verticis gyrata (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3737488018 | Primary non-essential cutis verticis gyrata | en | Synonym | Active | Case insensitive | SNOMED CT core |
3737489014 | A rare genetic dermis disorder with characteristics of slowly progressive thickening of the scalp, which becomes raised and forms ridges and furrows with symmetrical distribution resembling the cerebral gyri and cannot be flattened by traction or pressure, associated with ophthalmologic (for example congenital cataract) and/or neurological abnormalities (for example intellectual disability, epilepsy, microcephaly, encephalopathy). | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Primary non-essential cutis verticis gyrata | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
Primary non-essential cutis verticis gyrata | Finding site | Skin structure of scalp | true | Inferred relationship | Some | 1 | |
Primary non-essential cutis verticis gyrata | Is a | Cutis verticis gyrata | true | Inferred relationship | Some | ||
Primary non-essential cutis verticis gyrata | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set