Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 198876012 | Steely hair syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 198877015 | Menkes syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 198878013 | Kinky hair disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 498366018 | Congenital hypocupraemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 498367010 | MK - Menkes syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 498368017 | MNK - Menkes syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 498369013 | Steely hair disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 498370014 | Menke's kinky hair syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 797991018 | Menkes kinky-hair syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| 98318012 | Menkes kinky-hair syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 98319016 | Menkes disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 98320010 | Congenital hypocupremia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 98321014 | X-linked copper deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 98322019 | Copper transport disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 98323012 | Steely-hair syndrome | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 98324018 | Trichopoliodystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set