Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3315785016 | Primary pigmented nodular adrenocortical disease (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3315796012 | Primary pigmented nodular adrenocortical disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
3315797015 | Primary pigmented nodular adrenocortical disease (PPNAD) is a form of bilateral adrenocortical hyperplasia that is often associated with adrenocorticotrophin hormone independent Cushing syndrome. The disease has characteristics of small to normal sized adrenal glands containing multiple small cortical pigmented nodules. A substantial proportion of patients present during early childhood (2-3 years). More than 90% of reported cases of PPNAD occur as one of the manifestations of Carney complex. The condition is inherited in an autosomal dominant manner and can be associated with mutations in the PRKAR1A, PDE11A and PDE8B genes. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Primary pigmented nodular adrenocortical disease | Is a | Micronodular adrenal hyperplasia | true | Inferred relationship | Some | ||
Primary pigmented nodular adrenocortical disease | Associated morphology | Micronodular hyperplasia | true | Inferred relationship | Some | 1 | |
Primary pigmented nodular adrenocortical disease | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Primary pigmented nodular adrenocortical disease | Is a | Adrenocortical hyperplasia | false | Inferred relationship | Some | ||
Primary pigmented nodular adrenocortical disease | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Some | ||
Primary pigmented nodular adrenocortical disease | Associated morphology | Hyperplasia | false | Inferred relationship | Some | 1 | |
Primary pigmented nodular adrenocortical disease | Finding site | Adrenal cortex structure | true | Inferred relationship | Some | 1 | |
Primary pigmented nodular adrenocortical disease | Associated morphology | Hyperplasia | false | Inferred relationship | Some | 2 | |
Primary pigmented nodular adrenocortical disease | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Primary pigmented nodular adrenocortical disease | Finding site | Adrenal cortex structure | false | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set