197679002: Glomerular disease (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Viscus structure finding (finding)\Abdominal organ finding\Kidney finding\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease

\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of retroperitoneal compartment (disorder)\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of urinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Kidney finding\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disorder of abdomen (disorder)\Disorder of retroperitoneal compartment (disorder)\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disorder of abdomen (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Urinary system finding\Kidney finding\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Urinary system finding\Disorder of urinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disorder of the genitourinary system (disorder)\Disorder of urinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of retroperitoneal compartment (disorder)\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of urinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

303967017 Glomerular disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

582084011 Glomerular disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2837648015 Glomerulopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

960491000172117 néphropathie glomérulaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Glomerular disease	Is a	Kidney disease	false	Inferred relationship	Some
Glomerular disease	Finding site	Kidney structure	false	Inferred relationship	Some
Glomerular disease	Finding site	Glomerulus structure	true	Inferred relationship	Some	1
Glomerular disease	Is a	Disorder of renal parenchyma (disorder)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Glomerular disorders in neoplastic diseases	Is a	False	Glomerular disease	Inferred relationship	Some
Glomerular disorders in blood diseases and disorders involving the immune mechanism	Is a	True	Glomerular disease	Inferred relationship	Some
[X]Glomerular disorders in infectious and parasitic diseases classified elsewhere	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Glomerular disorders in neoplastic diseases classified elsewhere	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Glomerular disorders in blood diseases and disorders involving the immune mechanism classified elsewhere	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Glomerular disorders in diabetes mellitus	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Glomerular disorders in other endocrine, nutritional and metabolic diseases classified elsewhere	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Glomerular disorders in systemic disorders of connective tissue classified elsewhere	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Glomerular disorders in other diseases classified elsewhere	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Rapidly progressive nephritic syndrome, other	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Unspecified nephritic syndrome, minor glomerular abnormality	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Unspecified nephritic syndrome, diffuse mesangial proliferative glomerulonephritis	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Unspecified nephritic syndrome, diffuse endocapillary proliferative glomerulonephritis	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Unspecified nephritic syndrome, dense deposit disease	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Unspecified nephritic syndrome, diffuse concentric glomerulonephritis	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Isolated proteinuria, with other specified morphological changes	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Isolated proteinuria, with unspecified morphological changes	Is a	False	Glomerular disease	Inferred relationship	Some
[X]Hereditary nephropathy, unspecified morphological changes	Is a	False	Glomerular disease	Inferred relationship	Some
Nephritic syndrome	Is a	False	Glomerular disease	Inferred relationship	Some
Glomerulosclerosis	Is a	True	Glomerular disease	Inferred relationship	Some
Lipoprotein glomerulopathy (disorder)	Is a	True	Glomerular disease	Inferred relationship	Some
Glomerulonephritis	Is a	True	Glomerular disease	Inferred relationship	Some
syndrome de glomérulonéphrite hémorragique aiguë bénigne	Is a	False	Glomerular disease	Inferred relationship	Some
Nephrotic syndrome	Is a	True	Glomerular disease	Inferred relationship	Some
An idiopathic glomerular disease characterized by massive accumulation of atypical type III collagen fibrils within the mesangial matrix and subendothelial space of glomeruli.	Is a	True	Glomerular disease	Inferred relationship	Some
Juxtaglomerular hyperplasia co-occurrent with secondary hyperaldosteronism (disorder)	Is a	True	Glomerular disease	Inferred relationship	Some
Hereditary focal and segmental glomerular lesions	Is a	True	Glomerular disease	Inferred relationship	Some
Hereditary minor glomerular abnormality (disorder)	Is a	True	Glomerular disease	Inferred relationship	Some
Glomerular disease due to systemic lupus erythematosus (disorder)	Is a	False	Glomerular disease	Inferred relationship	Some
A rare hereditary motor and sensory neuropathy disorder characterized by the typical CMT phenotype (slowly progressive distal muscle weakness and atrophy in upper and lower limbs, distal sensory loss in extremities, reduced or absent deep tendon reflexes and foot deformities) associated with focal segmental glomerulosclerosis (manifesting with proteinuria and progression to end-stage renal disease). Mild or moderate sensorineural hearing loss may also be associated. Nerve biopsy reveals both axonal and demyelinating changes and nerve conduction velocities vary from the demyelinating to axonal range (typically between 25-50m/sec).	Is a	True	Glomerular disease	Inferred relationship	Some
Idiopathic glomerular disease (disorder)	Is a	True	Glomerular disease	Inferred relationship	Some
Glomerular disorder due to non-neuropathic heredofamilial amyloidosis (disorder)	Is a	False	Glomerular disease	Inferred relationship	Some
Necrosis of capillary of kidney due to glomerular disease (disorder)	Due to	True	Glomerular disease	Inferred relationship	Some	1
An extremely rare syndromic lymphedema disorder characterized by early-onset hypotrichosis, childhood-onset lymphedema, and variable telangiectasia, particularly of the palms.	Is a	True	Glomerular disease	Inferred relationship	Some
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.	Is a	True	Glomerular disease	Inferred relationship	Some
Ischaemic glomerulopathy	Is a	False	Glomerular disease	Inferred relationship	Some
Thin basement membrane disease	Is a	True	Glomerular disease	Inferred relationship	Some
A rare genetic cerebral small vessel disease characterized by progressive loss of visual acuity due to retinal vasculopathy, in combination with more variable neurological signs and symptoms including stroke, cognitive decline, migraine-like headaches, and seizures, among others, typically beginning in middle age. Psychiatric features such as depression and anxiety may also occur. Systemic vascular involvement with Raynaud phenomenon, micronodular liver cirrhosis, and glomerular kidney dysfunction is present in a subset of patients.	Is a	True	Glomerular disease	Inferred relationship	Some
Glomerulopathy due to diabetes mellitus (disorder)	Is a	False	Glomerular disease	Inferred relationship	Some
Goodpasture's disease	Is a	False	Glomerular disease	Inferred relationship	Some
Glomerular fibrosis (disorder)	Is a	True	Glomerular disease	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	True	Glomerular disease	Inferred relationship	Some
A rare, secondary glomerular disease characterized by proteinuria, dysproteinemias, nephrotic syndrome, and nodular glomerulopathy leading to renal failure, with or without extra-renal manifestations. The renal biopsy shows typical deposits of monoclonal immunoglobulins that do not show a fibrillar organization and are negative for Congo red staining. Associated signs and symptoms depend on the involvement of other organs, liver, heart, nerve fibers, gastrointestinal tract, or skin.	Is a	True	Glomerular disease	Inferred relationship	Some
Familial hematuria (disorder)	Is a	True	Glomerular disease	Inferred relationship	Some
Glomerular disease due to infectious disease (disorder)	Is a	False	Glomerular disease	Inferred relationship	Some
Glomerular disease due to Fabry disease	Is a	False	Glomerular disease	Inferred relationship	Some
Secondary glomerular disease	Is a	True	Glomerular disease	Inferred relationship	Some
Transplant glomerulopathy	Is a	True	Glomerular disease	Inferred relationship	Some
A rare multiple congenital anomalies/dysmorphic syndrome characterized by profound intellectual disability, choreoathetosis, progressive spastic diplegia, progressive tapetoretinal degeneration with loss of retinal vessels, and glomerulopathy resulting in death late in the first or early in the second decade of life. Absence of the cerebellar granular layer has been reported. There have been no further descriptions in the literature since 1982.	Is a	True	Glomerular disease	Inferred relationship	Some
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.	Is a	True	Glomerular disease	Inferred relationship	Some
Disorder of glomerulus caused by Plasmodium malariae (disorder)	Is a	True	Glomerular disease	Inferred relationship	Some
Multiple cysts of glomerulus of kidney (disorder)	Is a	True	Glomerular disease	Inferred relationship	Some

Reference Sets

Description inactivation indicator reference set

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Id	Description	Lang	Type	Status	Case?	Module
303967017	Glomerular disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
582084011	Glomerular disease (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2837648015	Glomerulopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
960491000172117	néphropathie glomérulaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module