722760002: Dense deposit disease (disorder)

\Viscus structure finding (finding)\Abdominal organ finding\Kidney finding\Kidney disease\...

\Hereditary nephropathy (disorder)\Hereditary nephritis (disorder)\A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.

\Disorder of renal parenchyma (disorder)\Glomerular disease\Glomerulonephritis\Proliferative glomerulonephritis\Chronic proliferative glomerulonephritis (disorder)\Chronic mesangial proliferative glomerulonephritis\Mesangiocapillary glomerulonephritis\Complement component 3 glomerulopathy (disorder)\A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.
\Disorder of renal parenchyma (disorder)\Glomerular disease\Glomerulonephritis\Hereditary nephritis (disorder)\A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.
\Disorder of renal parenchyma (disorder)\Glomerular disease\Glomerulonephritis\Mesangial proliferative glomerulonephritis\Chronic mesangial proliferative glomerulonephritis\Mesangiocapillary glomerulonephritis\Complement component 3 glomerulopathy (disorder)\A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.
\Disorder of renal parenchyma (disorder)\Glomerular disease\Glomerulonephritis\Chronic glomerulonephritis\Chronic proliferative glomerulonephritis (disorder)\Chronic mesangial proliferative glomerulonephritis\Mesangiocapillary glomerulonephritis\Complement component 3 glomerulopathy (disorder)\A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.
\Disorder of renal parenchyma (disorder)\Nephritis\Glomerulonephritis\Proliferative glomerulonephritis\Chronic proliferative glomerulonephritis (disorder)\Chronic mesangial proliferative glomerulonephritis\Mesangiocapillary glomerulonephritis\Complement component 3 glomerulopathy (disorder)\A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.
\Disorder of renal parenchyma (disorder)\Nephritis\Glomerulonephritis\Hereditary nephritis (disorder)\A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.
\Disorder of renal parenchyma (disorder)\Nephritis\Glomerulonephritis\Mesangial proliferative glomerulonephritis\Chronic mesangial proliferative glomerulonephritis\Mesangiocapillary glomerulonephritis\Complement component 3 glomerulopathy (disorder)\A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.
\Disorder of renal parenchyma (disorder)\Nephritis\Glomerulonephritis\Chronic glomerulonephritis\Chronic proliferative glomerulonephritis (disorder)\Chronic mesangial proliferative glomerulonephritis\Mesangiocapillary glomerulonephritis\Complement component 3 glomerulopathy (disorder)\A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

5402976014 A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5402977017 A histological subtype of C3 glomerulopathy characterised by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3333378011 Dense deposit disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3333379015 Dense deposit disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3758323019 Mesangiocapillary glomerulonephritis type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4652576012 Membranoproliferative glomerulonephritis type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4652578013 MPGNII - membranoproliferative glomerulonephritis type II en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

5244191012 MCGN (mesangiocapillary glomerulonephritis) type II en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

889121000172113 maladie de dépôt dense fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

976341000172113 glomérulonéphrite membranoproliférative type 2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3423281001000114 Glomerulonephritis, membranoproliferative, Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Is a	Complement component 3 glomerulopathy (disorder)	true	Inferred relationship	Some
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Clinical course	Chronic	true	Inferred relationship	Some	2
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Finding site	Glomerulus structure	false	Inferred relationship	Some	3
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Finding site	Glomerulus structure	false	Inferred relationship	Some	4
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Associated morphology	inflammation chronique	false	Inferred relationship	Some	3
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Associated morphology	Proliferative inflammation	false	Inferred relationship	Some	4
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Associated morphology	Chronic proliferative inflammation	true	Inferred relationship	Some	1
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Finding site	Glomerulus structure	false	Inferred relationship	Some	1
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Is a	Hereditary nephritis (disorder)	true	Inferred relationship	Some
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Is a	Mesangiocapillary glomerulonephritis	false	Inferred relationship	Some
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Finding site	Structure of glomerular mesangium	true	Inferred relationship	Some	1
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Causative agent (attribute)	Complement component C3	true	Inferred relationship	Some	3
A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Associated morphology	Complement component 3 deposit (morphologic abnormality)	true	Inferred relationship	Some	3

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Recurrent hematuria co-occurrent and due to dense deposit disease (disorder)	Due to	True	A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Inferred relationship	Some	1
Recurrent hematuria co-occurrent and due to dense deposit disease (disorder)	Is a	True	A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Inferred relationship	Some
Persistent hematuria co-occurrent and due to dense deposit disease (disorder)	Due to	True	A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Inferred relationship	Some	1
Persistent hematuria co-occurrent and due to dense deposit disease (disorder)	Is a	True	A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	Inferred relationship	Some

Reference Sets

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

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Id	Description	Lang	Type	Status	Case?	Module
5402976014	A histological subtype of C3 glomerulopathy characterized by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5402977017	A histological subtype of C3 glomerulopathy characterised by C3 deposition in renal tissue in the absence or near-absence of immunoglobulin deposits, in a patient with the classic clinical features of glomerulonephritis and electron microscopic findings of highly electron-dense intra-membranous, osmiophilic deposits.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3333378011	Dense deposit disease (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3333379015	Dense deposit disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3758323019	Mesangiocapillary glomerulonephritis type 2	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4652576012	Membranoproliferative glomerulonephritis type 2	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4652578013	MPGNII - membranoproliferative glomerulonephritis type II	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5244191012	MCGN (mesangiocapillary glomerulonephritis) type II	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
889121000172113	maladie de dépôt dense	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
976341000172113	glomérulonéphrite membranoproliférative type 2	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3423281001000114	Glomerulonephritis, membranoproliferative, Typ 2	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module