Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 203798012 | Deficiency of steroid 21-hydroxylase | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 203799016 | Deficiency of steroid 21-monooxygenase | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3332438012 | 21-hydroxylase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 473063012 | CAH - 21-hydroxylase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 727726019 | Deficiency of steroid 21-monooxygenase (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Deficiency of steroid 21-monooxygenase | Is a | Specific enzyme deficiency | true | Inferred relationship | Some | ||
| Deficiency of steroid 21-monooxygenase | Is a | Congenital adrenal hyperplasia | false | Inferred relationship | Some | ||
| Deficiency of steroid 21-monooxygenase | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Deficiency of steroid 21-monooxygenase | Is a | Disorder of adrenal cortex | true | Inferred relationship | Some | ||
| Deficiency of steroid 21-monooxygenase | Is a | Disorder of steroid metabolism | true | Inferred relationship | Some | ||
| Deficiency of steroid 21-monooxygenase | Finding site | Entire endocrine gonad | false | Inferred relationship | Some | ||
| Deficiency of steroid 21-monooxygenase | Finding site | Adrenal cortex structure | true | Inferred relationship | Some | 1 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set