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818952002: Fibronectin glomerulopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5408830019 A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5408831015 A primary glomerular disease characterised by proteinuria, type IV renal tubular acidosis, microscopic haematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3856295011 Fibronectin glomerulopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3856296012 Glomerulopathy with fibronectin deposits en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3856297015 Fibronectin glomerulopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6158351000241118 glomérulopathie à dépôts de fibronectine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3428231001000115 Fibronektin-Glomerulopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. Is a Autosomal dominant hereditary disorder (disorder) true Inferred relationship Some
A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. Is a Hereditary nephropathy (disorder) true Inferred relationship Some
A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. Is a Renal disorders in inherited disease false Inferred relationship Some
A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. Is a Glomerular disease true Inferred relationship Some
A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. Finding site Glomerulus structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Glomerulopathy with giant fibrillar deposits (disorder) Is a True A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. Inferred relationship Some
Glomerulopathy with fibronectin deposits 2 (disorder) Is a True A primary glomerular disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. Inferred relationship Some

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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