Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3700751016 | Alport syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3700752011 | Alport syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5404782017 | A rare renal disease characterized by glomerular nephropathy with hematuria progressing to end-stage renal disease (ESRD), frequently associated with sensorineural deafness, and occasionally with ocular anomalies. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5404783010 | A rare renal disease characterised by glomerular nephropathy with haematuria progressing to end-stage renal disease (ESRD), frequently associated with sensorineural deafness, and occasionally with ocular anomalies. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Alport syndrome (disorder) | Associated morphology | Chronic inflammation | false | Inferred relationship | Some | 1 | |
Alport syndrome (disorder) | Interprets | Hearing | true | Inferred relationship | Some | 3 | |
Alport syndrome (disorder) | Is a | Hereditary nephritis (disorder) | true | Inferred relationship | Some | ||
Alport syndrome (disorder) | Finding site | Structure of auditory system (body structure) | true | Inferred relationship | Some | 2 | |
Alport syndrome (disorder) | Finding site | Glomerulus structure | true | Inferred relationship | Some | 1 | |
Alport syndrome (disorder) | Is a | Sensorineural hearing loss | true | Inferred relationship | Some | ||
Alport syndrome (disorder) | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
Alport syndrome (disorder) | Associated morphology | Chronic inflammatory morphology (morphologic abnormality) | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Alport syndrome autosomal recessive (disorder) | Is a | True | Alport syndrome (disorder) | Inferred relationship | Some | |
Alport syndrome X-linked (disorder) | Is a | True | Alport syndrome (disorder) | Inferred relationship | Some | |
Alport syndrome autosomal dominant (disorder) | Is a | True | Alport syndrome (disorder) | Inferred relationship | Some | |
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder) | Is a | False | Alport syndrome (disorder) | Inferred relationship | Some | |
Glomerular disease due to Alport syndrome | Due to | True | Alport syndrome (disorder) | Inferred relationship | Some | 2 |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)