Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3444192017 | Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3444193010 | Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3444194016 | Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunisation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5403496015 | A rare, congenital glomerular disease due to maternal anti-neutral endopeptidase (NEP) alloimmunization characterized by severe renal failure and nephrotic syndrome at birth, which rapidly improves in the first weeks of life. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403497012 | A rare, congenital glomerular disease due to maternal anti-neutral endopeptidase (NEP) alloimmunisation characterised by severe renal failure and nephrotic syndrome at birth, which rapidly improves in the first weeks of life. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3444192017 | Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3444193010 | Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3444194016 | Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunisation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3444195015 | A glomerular disease with characteristics of severe renal failure and nephrotic syndrome at birth, which rapidly improves in the first weeks of life. The disorder has been described in 15 infants from 5 families originating from Portugal, the Netherlands, Italy, Germany and Morocco. The disease is a congenital disorder where infants present at birth with nephrotic syndrome, acute renal failure (oligoanuria and proteinuria), or both. Respiratory distress and hypertension are also observed during the first days of life. Some degree of dysmorphism may be observed in some cases. Mothers do not show any renal manifestations. Caused by the transplacental transfer of nephritogenic anti-NEP antibodies (IgG1, IgG4 subtypes) from mothers with truncating mutations of the MME gene (3q25.2; coding for NEP), resulting in a functional knockout of MME. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403496015 | A rare, congenital glomerular disease due to maternal anti-neutral endopeptidase (NEP) alloimmunization characterized by severe renal failure and nephrotic syndrome at birth, which rapidly improves in the first weeks of life. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403497012 | A rare, congenital glomerular disease due to maternal anti-neutral endopeptidase (NEP) alloimmunisation characterised by severe renal failure and nephrotic syndrome at birth, which rapidly improves in the first weeks of life. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3420651001000113 | Kongenitale membranöse Nephropathie durch Alloimmunisierung gegen fetomaternale anti-neutrale Endopeptidase | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5905401000241114 | FMAIG - fetomaternal alloimmunization with antenatal glomerulopathies | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5905411000241111 | glomérulopathie extramembraneuse congénitale par allo-immunisation fœtomaternelle anti-endopeptidase neutre | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5905421000241116 | GEM (glomérulopathie extramembraneuse) allo-immune | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5905401000241114 | FMAIG - fetomaternal alloimmunization with antenatal glomerulopathies | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5905411000241111 | glomérulopathie extramembraneuse congénitale par allo-immunisation fœtomaternelle anti-endopeptidase neutre | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5905421000241116 | GEM (glomérulopathie extramembraneuse) allo-immune | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3420651001000113 | Kongenitale membranöse Nephropathie durch Alloimmunisierung gegen fetomaternale anti-neutrale Endopeptidase | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization (disorder) | Is a | Congenital disease | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization (disorder) | Is a | Glomerular disease | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization (disorder) | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization (disorder) | Finding site | Glomerulus structure (body structure) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)