Status: current, Defined. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
154259018 | Congenital hypoplasia of adrenal gland | en | Synonym | Active | Case insensitive | SNOMED CT core |
154260011 | Congenital small adrenal gland | en | Synonym | Active | Case insensitive | SNOMED CT core |
510260012 | Congenital adrenal hypoplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
510261011 | CAH - Congenital adrenal hypoplasia | en | Synonym | Active | Case sensitive | SNOMED CT core |
836926011 | Congenital hypoplasia of adrenal gland (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Familial adrenal hypoplasia with absent pituitary luteinising hormone | Is a | True | Congenital hypoplasia of adrenal gland | Inferred relationship | Some | |
Familial steroid-resistant nephrotic syndrome with adrenal insufficiency | Is a | True | Congenital hypoplasia of adrenal gland | Inferred relationship | Some | |
MIRAGE syndrome | Is a | False | Congenital hypoplasia of adrenal gland | Inferred relationship | Some | |
MIRAGE syndrome | Is a | True | Congenital hypoplasia of adrenal gland | Inferred relationship | Some | |
Congenital adrenal hypoplasia, X-linked | Is a | True | Congenital hypoplasia of adrenal gland | Inferred relationship | Some | |
Familial adrenocortical hypoplasia | Is a | True | Congenital hypoplasia of adrenal gland | Inferred relationship | Some | |
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency | Is a | True | Congenital hypoplasia of adrenal gland | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set