Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2017. Module: SNOMED CT Netherlands NRC maintained module (core metadata concept)
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
194381000146112 | Congenital nephrotic syndrome due to WT-1 mutation (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
194391000146114 | Congenital nephrotic syndrome due to WT-1 mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
712311000146118 | congenitaal nefrotisch syndroom WT1 mutatie (aandoening) | nl | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
712321000146111 | congenitaal nefrotisch syndroom WT1 mutatie | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital nephrotic syndrome due to WT-1 mutation (disorder) | Is a | Congenital nephrotic syndrome | true | Inferred relationship | Some | ||
Congenital nephrotic syndrome due to WT-1 mutation (disorder) | Due to | Genetic mutation | true | Inferred relationship | Some | 4 | |
Congenital nephrotic syndrome due to WT-1 mutation (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Congenital nephrotic syndrome due to WT-1 mutation (disorder) | Finding site | Glomerulus structure | false | Inferred relationship | Some | 2 | |
Congenital nephrotic syndrome due to WT-1 mutation (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Congenital nephrotic syndrome due to WT-1 mutation (disorder) | Interprets | Measurement of protein in urine (procedure) | true | Inferred relationship | Some | 3 | |
Congenital nephrotic syndrome due to WT-1 mutation (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital nephrotic syndrome due to WT-1 mutation (disorder) | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
Congenital nephrotic syndrome due to WT-1 mutation (disorder) | Finding site | Glomerulus structure | true | Inferred relationship | Some | 1 | |
Congenital nephrotic syndrome due to WT-1 mutation (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital nephrotic syndrome due to WT-1 mutation (disorder) | Interprets | Albumin measurement | true | Inferred relationship | Some | 2 | |
Congenital nephrotic syndrome due to WT-1 mutation (disorder) | Has interpretation | Above reference range | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets