Status: current, 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 |
3331711016 | Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3331712011 | Congenital nephrotic syndrome due to diffuse mesangial sclerosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3331713018 | Congenital nephrotic syndrome (CNS) due to diffuse mesangial sclerosis | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3331714012 | Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3331711016 | Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3331711016 | Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3331712011 | Congenital nephrotic syndrome due to diffuse mesangial sclerosis | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3331712011 | Congenital nephrotic syndrome due to diffuse mesangial sclerosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3331713018 | Congenital nephrotic syndrome (CNS) due to diffuse mesangial sclerosis | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3331714012 | Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5905241000241113 | syndrome néphrotique congénital dû à une sclérose mésangiale diffuse | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5905251000241111 | syndrome néphrotique congénital dû à une sclérose diffuse du mésangium | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5905241000241113 | syndrome néphrotique congénital dû à une sclérose mésangiale diffuse | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5905251000241111 | syndrome néphrotique congénital dû à une sclérose diffuse du mésangium | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | Due to | Diffuse mesangial sclerosis | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 4 | |
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | Is a | Congenital nephrotic syndrome | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | Is a | Nephrotic syndrome associated with another disorder (disorder) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 | |
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | Finding site | Glomerulus structure (body structure) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 | |
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | Is a | Hereditary nephropathy (disorder) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | Is a | Congenital disease | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | Has interpretation | Above reference range | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | Interprets | Albumin measurement (procedure) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 3 | |
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | Interprets | Measurement of protein in urine (procedure) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | Has interpretation | Below reference range | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 3 | |
Congenital nephrotic syndrome with evidence of diffuse mesangial sclerosis on histology or with DNA evidence of a genetic mutation associated with diffuse mesangial sclerosis. | Is a | Glomerular disease due to diffuse mesangial sclerosis | true | Inferred relationship | Existential restriction modifier (core metadata concept) |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets