Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 123510010 | Micromelia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 123512019 | Micromelus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 123513012 | Micromelic dwarf | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 123515017 | Nanomelia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 814861012 | Micromelia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Microlissencephaly micromelia syndrome (disorder) | Is a | True | Micromelia | Inferred relationship | Some | |
| Short rib polydactyly syndrome type I (disorder) | Is a | True | Micromelia | Inferred relationship | Some | |
| Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder) | Is a | True | Micromelia | Inferred relationship | Some | |
| 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 (disorder) | Is a | True | Micromelia | Inferred relationship | Some | |
| Short rib polydactyly syndrome type 5 | Is a | True | Micromelia | Inferred relationship | Some |
This concept is not in any reference sets
FHIR