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725592009: Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization (disorder)


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


0 descendants.

Expanded Value Set


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)

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