Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2981453012 | CYP21 deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2981456016 | 21-hydroxylase deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2981467015 | 21-hydroxylase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| 21-hydroxylase deficiency (disorder) | est un(e) (attribut) | Adrenogenital disorder | false | Inferred relationship | Some | ||
| 21-hydroxylase deficiency (disorder) | est un(e) (attribut) | Hereditary disorder of endocrine system (disorder) | false | Inferred relationship | Some | ||
| 21-hydroxylase deficiency (disorder) | est un(e) (attribut) | Disorder of steroid metabolism | false | Inferred relationship | Some | ||
| 21-hydroxylase deficiency (disorder) | est un(e) (attribut) | Specific enzyme deficiency | false | Inferred relationship | Some | ||
| 21-hydroxylase deficiency (disorder) | est un(e) (attribut) | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
| 21-hydroxylase deficiency (disorder) | localisation d'une constatation (attribut) | glande suprarénale | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Steroid 21-monooxygenase deficiency, simple virilising type | Due to | False | 21-hydroxylase deficiency (disorder) | Inferred relationship | Some | |
| Steroid 21-monooxygenase deficiency, salt wasting type | Due to | False | 21-hydroxylase deficiency (disorder) | Inferred relationship | Some | |
| hyperplasie congénitale des surrénales par déficit en 21-hydroxylase classique | Due to | False | 21-hydroxylase deficiency (disorder) | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
SAME AS association reference set (foundation metadata concept)
FHIR