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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Glomerular disease	Is a	Kidney disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerular disease	Finding site	Kidney structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerular disease	Finding site	Glomerulus structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Glomerular disease	Is a	Disorder of renal parenchyma (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Glomerular disorders in neoplastic diseases	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerular disorders in blood diseases and disorders involving the immune mechanism	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Glomerular disorders in infectious and parasitic diseases classified elsewhere	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Glomerular disorders in neoplastic diseases classified elsewhere	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Glomerular disorders in blood diseases and disorders involving the immune mechanism classified elsewhere	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Glomerular disorders in diabetes mellitus	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Glomerular disorders in other endocrine, nutritional and metabolic diseases classified elsewhere	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Glomerular disorders in systemic disorders of connective tissue classified elsewhere	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Glomerular disorders in other diseases classified elsewhere	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Rapidly progressive nephritic syndrome, other	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Unspecified nephritic syndrome, minor glomerular abnormality	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Unspecified nephritic syndrome, diffuse mesangial proliferative glomerulonephritis	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Unspecified nephritic syndrome, diffuse endocapillary proliferative glomerulonephritis	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Unspecified nephritic syndrome, dense deposit disease	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Unspecified nephritic syndrome, diffuse concentric glomerulonephritis	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Isolated proteinuria, with other specified morphological changes	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Isolated proteinuria, with unspecified morphological changes	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
[X]Hereditary nephropathy, unspecified morphological changes	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Nephritic syndrome	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerulosclerosis	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Lipoprotein glomerulopathy (disorder)	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerulonephritis	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
syndrome de glomérulonéphrite hémorragique aiguë bénigne	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Nephrotic syndrome	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Collagenofibrotic glomerulopathy (disorder)	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Juxtaglomerular hyperplasia co-occurrent with secondary hyperaldosteronism (disorder)	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary focal and segmental glomerular lesions (disorder)	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary minor glomerular abnormality	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerular disease due to systemic lupus erythematosus	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
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	Existential restriction modifier (core metadata concept)
Idiopathic glomerular disease (disorder)	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerular disorder due to non-neuropathic heredofamilial amyloidosis (disorder)	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Necrosis of capillary of kidney due to glomerular disease (disorder)	Due to	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)	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	Existential restriction modifier (core metadata concept)
Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization (disorder)	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerulopathy due to ischemia (disorder)	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Thin basement membrane disease (disorder)	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerulopathy due to diabetes mellitus (disorder)	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Goodpasture's disease	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerular fibrosis (disorder)	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
A primary glomerular disease with characteristics of 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. Fibronectin glomerulopathy may present at different ages, although mostly in adolescence or early adulthood, with typical features of a nephrotic syndrome including hypertension. Clustering of the disease within families indicates a genetic origin. In 40% of families, the disease is caused by heterozygous mutations in the FN1 gene (2q34) encoding fibronectin. Whole-genome linkage analysis in a large pedigree showed another disease locus on 1q32, however no specific candidate genes has been identified so far. Segregation with disease appearance in successive generations is consistent with an autosomal dominant pattern of inheritance with age-related penetrance.	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Non-amyloid monoclonal immunoglobulin deposition disease (disorder)	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial hematuria	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerular disease due to infectious disease (disorder)	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerular disease due to Fabry disease (disorder)	Is a	False	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Secondary disorder of glomerulus (disorder)	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Transplant glomerulopathy	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Severe oculo-renal-cerebellar syndrome (disorder)	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Idiopathic non-lupus full-house nephropathy (disorder)	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)
Disorder of glomerulus caused by Plasmodium malariae	Is a	True	Glomerular disease	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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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
303967017	Glomerular disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character 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	Only initial character 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
960491000172117	néphropathie glomérulaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module