Status: current, Primitive. Date: 31-Jul 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3902186018 | Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3902187010 | Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form | Is a | Disorder of adrenal cortex | false | Inferred relationship | Some | ||
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form | Is a | Congenital anomaly of adrenal gland | true | Inferred relationship | Some | ||
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form | Finding site | Adrenal cortex structure | true | Inferred relationship | Some | 1 | |
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form | Associated morphology | Hyperplasia | true | Inferred relationship | Some | 1 | |
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form | Due to | Deficiency of steroid 21-monooxygenase | true | Inferred relationship | Some | 2 | |
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form | Is a | Adrenocortical hyperplasia | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set