Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 39577015 | Glucoaminophosphaturia syndrome with rickets | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 753104014 | Glucoaminophosphaturia syndrome with rickets (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 |
| Glucoaminophosphaturia syndrome with rickets | Is a | Hereditary disorder of musculoskeletal system | false | Inferred relationship | Some | ||
| Glucoaminophosphaturia syndrome with rickets | Is a | Congenital anomaly of cartilage | false | Inferred relationship | Some | ||
| Glucoaminophosphaturia syndrome with rickets | Is a | Congenital anomaly of skeletal bone | false | Inferred relationship | Some | ||
| Glucoaminophosphaturia syndrome with rickets | Is a | Glucoaminophosphaturia syndrome | false | Inferred relationship | Some | ||
| Glucoaminophosphaturia syndrome with rickets | Is a | Rickets | false | Inferred relationship | Some | ||
| Glucoaminophosphaturia syndrome with rickets | Finding site | Osteoid tissue | false | Inferred relationship | Some | 1 | |
| Glucoaminophosphaturia syndrome with rickets | Finding site | Cartilaginous tissue structure | false | Inferred relationship | Some | ||
| Glucoaminophosphaturia syndrome with rickets | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Glucoaminophosphaturia syndrome with rickets | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
| Glucoaminophosphaturia syndrome with rickets | Is a | Congenital connective tissue disorder | false | Inferred relationship | Some | ||
| Glucoaminophosphaturia syndrome with rickets | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR