Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3657944013 | Autosomal dominant polycystic kidney disease (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3657945014 | Autosomal dominant polycystic kidney disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3657946010 | ADPKD - autosomal dominant polycystic kidney disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 767791000241113 | polykystose rénale autosomique dominante (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 873291000172114 | polykystose rénale autosomique dominante | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 889621000172116 | ADPKD - autosomal dominant polycystic kidney disease | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3657947018 | Inherited disease with characteristics of the development of cysts in the kidneys. The disease rarely causes any noticeable problems until the cysts grow large enough to affect renal function, usually between 30 and 60 years of age. Less commonly, children or older people may have noticeable symptoms. Two different genes are known to cause this disease PKD1 and PKD2. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant polycystic kidney disease (disorder) | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Autosomal dominant polycystic kidney disease (disorder) | localisation d'une constatation (attribut) | structure d'un rein | true | Inferred relationship | Some | 1 | |
| Autosomal dominant polycystic kidney disease (disorder) | est un(e) (attribut) | Multiple congenital cysts of kidney | true | Inferred relationship | Some | ||
| Autosomal dominant polycystic kidney disease (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Autosomal dominant polycystic kidney disease (disorder) | morphologie associée (attribut) | Polycystic change | true | Inferred relationship | Some | 1 | |
| Autosomal dominant polycystic kidney disease (disorder) | est un(e) (attribut) | Hereditary nephropathy (disorder) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Multinodular goiter, cystic kidney, polydactyly syndrome (disorder) | est un(e) (attribut) | True | Autosomal dominant polycystic kidney disease (disorder) | Inferred relationship | Some | |
| Adult type polycystic kidney disease type 2 (disorder) | est un(e) (attribut) | True | Autosomal dominant polycystic kidney disease (disorder) | Inferred relationship | Some | |
| Adult type polycystic kidney disease type 1 | est un(e) (attribut) | True | Autosomal dominant polycystic kidney disease (disorder) | Inferred relationship | Some | |
| Autosomal dominant polycystic kidney disease in childhood | est un(e) (attribut) | True | Autosomal dominant polycystic kidney disease (disorder) | Inferred relationship | Some | |
| polykystose rénale autosomique dominante type 1 avec sclérose tubéreuse | est un(e) (attribut) | True | Autosomal dominant polycystic kidney disease (disorder) | Inferred relationship | Some |
Reference Sets
FHIR