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

722760002: Dense deposit disease (disorder)

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
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
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 Only initial character case insensitive (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 Only initial character 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
4652577015 MCGN type II - mesangiocapillary glomerulonephritis type II en Synonym (core metadata concept) Active Entire term case sensitive (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
4652594018 A histological subtype of C3 glomerulopathy with characteristics of 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
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
3423281001000114 Glomerulonephritis, membranoproliferative, Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
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
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

2 descendants. Search Descendants:

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 Existential restriction modifier (core metadata concept)
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 (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 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 (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 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 (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept) 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 (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 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 true Inferred relationship Existential restriction modifier (core metadata concept)
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 Existential restriction modifier (core metadata concept)
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 Existential restriction modifier (core metadata concept)
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 (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 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 (substance) true Inferred relationship Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept) 3
Inbound Relationships Type Active Source Characteristic Refinability Group
Recurrent hematuria co-occurrent and due to dense deposit disease 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 Existential restriction modifier (core metadata concept) 1
Recurrent hematuria co-occurrent and due to dense deposit disease 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 Existential restriction modifier (core metadata concept)
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 Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept)

Reference Sets

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

Back to Start