Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3315796012 | Primary pigmented nodular adrenocortical disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3886791000052116 | primär pigmenterad nodulär sjukdom i binjurebarken | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Primary pigmented nodular adrenocortical disease (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Primary pigmented nodular adrenocortical disease (disorder) | Is a | Adrenocortical hyperplasia | false | Inferred relationship | Some | ||
Primary pigmented nodular adrenocortical disease (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
Primary pigmented nodular adrenocortical disease (disorder) | Associated morphology | Hyperplasia | false | Inferred relationship | Some | 1 | |
Primary pigmented nodular adrenocortical disease (disorder) | Finding site | Adrenal cortex structure | true | Inferred relationship | Some | 1 | |
Primary pigmented nodular adrenocortical disease (disorder) | Associated morphology | Hyperplasia | false | Inferred relationship | Some | 2 | |
Primary pigmented nodular adrenocortical disease (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Primary pigmented nodular adrenocortical disease (disorder) | Finding site | Adrenal cortex structure | false | Inferred relationship | Some | 2 | |
Primary pigmented nodular adrenocortical disease (disorder) | Is a | Micronodular adrenal hyperplasia | true | Inferred relationship | Some | ||
Primary pigmented nodular adrenocortical disease (disorder) | Associated morphology | Micronodular hyperplasia (morphologic abnormality) | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets