Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 36865015 | Hereditary vitamin D dependency syndrome, type I | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 36866019 | ARUDD-I | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 36868018 | Hereditary selective AND simple deficiency of 1 alpha, 25(OH)>2< D | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 751327017 | Hereditary vitamin D dependency syndrome, type I (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary vitamin D dependency syndrome, type I | Is a | Hereditary vitamin D dependency syndrome | false | Inferred relationship | Some | ||
| Hereditary vitamin D dependency syndrome, type I | Finding site | Entire endocrine gonad (body structure) | false | Inferred relationship | Some | ||
| Hereditary vitamin D dependency syndrome, type I | Finding site | Structure of endocrine system (body structure) | false | Inferred relationship | Some | ||
| Hereditary vitamin D dependency syndrome, type I | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Hereditary vitamin D dependency syndrome, type I | Finding site | Structure of endocrine system (body structure) | false | Inferred relationship | Some | 1 |
| 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