Status: current, Defined. Date: 31-Jul 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 123510010 | Micromelia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 123511014 | Micromelia, NOS | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 123512019 | Micromelus | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 123513012 | Micromelic dwarf | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 123514018 | Nanomelia, NOS | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 123515017 | Nanomelia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 814861012 | Micromelia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Diastrophic dysplasia | Is a | True | Micromelia | Inferred relationship | Some | |
| Micromelic dwarfism Fryn type | Is a | True | Micromelia | Inferred relationship | Some | |
| Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome | Is a | True | Micromelia | Inferred relationship | Some | |
| Microlissencephaly micromelia syndrome | Is a | True | Micromelia | Inferred relationship | Some | |
| Short rib polydactyly syndrome Saldino Noonan type | Is a | True | Micromelia | Inferred relationship | Some | |
| Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome | Is a | True | Micromelia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set