FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

1260197005: Idiopathic non-lupus full-house nephropathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5159675019 Idiopathic non-lupus full-house nephropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5159676018 Idiopathic non-lupus full-house nephropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5159677010 Idiopathic non-lupus FHN (full-house nephropathy) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5400430013 A rare idiopathic glomerular clinical syndrome characterized by diffuse renal lesions that are indistinguishable from the lesions observed in systemic lupus erythematosus (SLE) in the absence of circulating autoantibodies and other systemic features necessary to meet the classification criteria for SLE. Patients may present with nephrotic syndrome, abnormal urinary sediment, acute renal insufficiency, progressive glomerulonephritis, and hypertension. Some patients have been reported to develop a progression to SLE over time. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400431012 A rare idiopathic glomerular clinical syndrome characterised by diffuse renal lesions that are indistinguishable from the lesions observed in systemic lupus erythematosus (SLE) in the absence of circulating autoantibodies and other systemic features necessary to meet the classification criteria for SLE. Patients may present with nephrotic syndrome, abnormal urinary sediment, acute renal insufficiency, progressive glomerulonephritis, and hypertension. Some patients have been reported to develop a progression to SLE over time. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5159675019 Idiopathic non-lupus full-house nephropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5159676018 Idiopathic non-lupus full-house nephropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5159677010 Idiopathic non-lupus FHN (full-house nephropathy) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5159678017 A rare idiopathic glomerular clinical syndrome with characteristics of diffuse renal lesions that are indistinguishable from the lesions observed in systemic lupus erythematosus (SLE) in the absence of circulating autoantibodies and other systemic features necessary to meet the classification criteria for SLE. Patients may present with nephrotic syndrome, abnormal urinary sediment, acute renal insufficiency, progressive glomerulonephritis and hypertension. Some patients have been reported to develop a progression to SLE over time. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400430013 A rare idiopathic glomerular clinical syndrome characterized by diffuse renal lesions that are indistinguishable from the lesions observed in systemic lupus erythematosus (SLE) in the absence of circulating autoantibodies and other systemic features necessary to meet the classification criteria for SLE. Patients may present with nephrotic syndrome, abnormal urinary sediment, acute renal insufficiency, progressive glomerulonephritis, and hypertension. Some patients have been reported to develop a progression to SLE over time. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400431012 A rare idiopathic glomerular clinical syndrome characterised by diffuse renal lesions that are indistinguishable from the lesions observed in systemic lupus erythematosus (SLE) in the absence of circulating autoantibodies and other systemic features necessary to meet the classification criteria for SLE. Patients may present with nephrotic syndrome, abnormal urinary sediment, acute renal insufficiency, progressive glomerulonephritis, and hypertension. Some patients have been reported to develop a progression to SLE over time. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Idiopathic non-lupus full-house nephropathy (disorder) Is a Glomerular disease true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic non-lupus full-house nephropathy (disorder) Is a Idiopathic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic non-lupus full-house nephropathy (disorder) Is a Kidney lesion true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic non-lupus full-house nephropathy (disorder) Finding site Glomerulus structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic non-lupus full-house nephropathy (disorder) Associated morphology Lesion 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)

Back to Start