Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1783827016 | Steroid 21-hydroxylase deficiency, simple virilising type | en | Synonym | Active | Case insensitive | SNOMED CT core |
1784215016 | Steroid 21-hydroxylase deficiency, simple virilizing type | en | Synonym | Active | Case insensitive | SNOMED CT core |
496368011 | Steroid 21-monooxygenase deficiency, simple virilising type | en | Synonym | Active | Case insensitive | SNOMED CT core |
496369015 | Simple-virilising congenital adrenal hyperplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
496370019 | Simple virilising adrenal hyperplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
496372010 | Simple-virilizing congenital adrenal hyperplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
790632010 | Steroid 21-monooxygenase deficiency, simple virilizing type (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
87546013 | Steroid 21-monooxygenase deficiency, simple virilizing type | en | Synonym | Active | Case insensitive | SNOMED CT core |
87548014 | Simple virilizing adrenal hyperplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
87549018 | Adrenogenital disorder due to 21-hydroxylase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
87550018 | Congenital adrenal hyperplasia, type 1 | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Steroid 21-monooxygenase deficiency, simple virilising type | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Steroid 21-monooxygenase deficiency, simple virilising type | Associated morphology | Hyperplasia | true | Inferred relationship | Some | 1 | |
Steroid 21-monooxygenase deficiency, simple virilising type | Is a | Congenital anomaly of trunk | false | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Is a | Congenital anomaly of adrenal gland | false | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Is a | Inborn error of metabolism | false | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Is a | Adrenal virilism | false | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Is a | Enzymopathy | false | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Is a | Hereditary disorder of endocrine system | false | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Is a | Congenital adrenal hyperplasia | false | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Is a | Reproductive system hereditary disorder | false | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Is a | Virilising syndrome of adrenal origin | true | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Is a | Disorder of steroid metabolism | false | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Associated morphology | Congenital hyperplasia | false | Inferred relationship | Some | 3 | |
Steroid 21-monooxygenase deficiency, simple virilising type | Finding site | Adrenal cortex structure | false | Inferred relationship | Some | 1 | |
Steroid 21-monooxygenase deficiency, simple virilising type | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Steroid 21-monooxygenase deficiency, simple virilising type | Associated morphology | Hyperplasia | false | Inferred relationship | Some | 2 | |
Steroid 21-monooxygenase deficiency, simple virilising type | Finding site | Adrenal cortex structure | false | Inferred relationship | Some | 3 | |
Steroid 21-monooxygenase deficiency, simple virilising type | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Steroid 21-monooxygenase deficiency, simple virilising type | Finding site | Adrenal cortex structure | true | Inferred relationship | Some | 1 | |
Steroid 21-monooxygenase deficiency, simple virilising type | Due to | 21-hydroxylase deficiency | false | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Is a | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | true | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Due to | Deficiency of steroid 21-monooxygenase | true | Inferred relationship | Some | 2 | |
Steroid 21-monooxygenase deficiency, simple virilising type | Associated morphology | Congenital hyperplasia | false | Inferred relationship | Some | 1 | |
Steroid 21-monooxygenase deficiency, simple virilising type | Finding site | Entire endocrine gonad | false | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Occurrence | Congenital | false | Inferred relationship | Some | ||
Steroid 21-monooxygenase deficiency, simple virilising type | Finding site | Adrenal cortex structure | false | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Mild steroid 21-hydroxylase deficiency | Is a | False | Steroid 21-monooxygenase deficiency, simple virilising type | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set