Status: current, Defined. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3006545013 | Congenital anomaly of the eyebrow | en | Synonym | Active | Case insensitive | SNOMED CT core |
377103012 | Congenital malformation of the eyebrow | en | Synonym | Active | Case insensitive | SNOMED CT core |
643937015 | Congenital malformation of the eyebrow (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome | Is a | False | Congenital malformation of the eyebrow | Inferred relationship | Some | |
Eyebrow duplication syndactyly syndrome | Is a | True | Congenital malformation of the eyebrow | Inferred relationship | Some | |
Synophrys | Is a | True | Congenital malformation of the eyebrow | Inferred relationship | Some | |
Absent eyebrow | Is a | True | Congenital malformation of the eyebrow | Inferred relationship | Some | |
Double eyebrow | Is a | True | Congenital malformation of the eyebrow | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set