Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 137435012 | Sex-linked hereditary disorder | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 137436013 | Sex-linked hereditary disorder, NOS | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 693631000077118 | trouble héréditaire lié au sexe (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 71211000077114 | trouble héréditaire lié au sexe | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 824362013 | Sex-linked hereditary disorder (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Sex-linked hereditary disorder | est un(e) (attribut) | maladie héréditaire | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Macular retinoschisis | est un(e) (attribut) | True | Sex-linked hereditary disorder | Inferred relationship | Some | |
| X-linked hereditary disease | est un(e) (attribut) | True | Sex-linked hereditary disorder | Inferred relationship | Some | |
| X chromosome-linked pyridoxine refractory sideroblastic anemia | est un(e) (attribut) | False | Sex-linked hereditary disorder | Inferred relationship | Some | |
| Ornithine carbamoyltransferase deficiency | est un(e) (attribut) | True | Sex-linked hereditary disorder | Inferred relationship | Some | |
| Opitz-Frias syndrome | est un(e) (attribut) | True | Sex-linked hereditary disorder | Inferred relationship | Some | |
| Juvenile retinoschisis | est un(e) (attribut) | False | Sex-linked hereditary disorder | Inferred relationship | Some | |
| Familial chondromalacia of patella (disorder) | est un(e) (attribut) | False | Sex-linked hereditary disorder | Inferred relationship | Some |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR