Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 78444018 | Hereditary vitamin D dependency syndrome type, II | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 78445017 | Hereditary generalized resistance to 1 alpha, 25(OH)>2< D | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 78446016 | ARUDD-II | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 494745015 | Hereditary generalised resistance to 1 alpha, 25(OH)>2< D | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 784480014 | Hereditary vitamin D dependency syndrome type, II (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary vitamin D dependency syndrome type, II | Is a | Hereditary vitamin D dependency syndrome | false | Inferred relationship | Existential restriction modifier | ||
| Hereditary vitamin D dependency syndrome type, II | Finding site | Entire endocrine gonad | false | Inferred relationship | Existential restriction modifier | ||
| Hereditary vitamin D dependency syndrome type, II | Finding site | Structure of endocrine system | false | Inferred relationship | Existential restriction modifier | ||
| Hereditary vitamin D dependency syndrome type, II | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 1 | |
| Hereditary vitamin D dependency syndrome type, II | Finding site | Structure of endocrine system | false | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR