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

399340005: Hereditary nephritis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1767260016 Hereditary nephritis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1778791010 Hereditary nephritis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786827012 GN - Hereditary glomerulonephritis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786828019 Hereditary glomerulonephritis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1767260016 Hereditary nephritis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1767260016 Hereditary nephritis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1778791010 Hereditary nephritis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1778791010 Hereditary nephritis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786827012 GN - Hereditary glomerulonephritis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786828019 Hereditary glomerulonephritis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786828019 Hereditary glomerulonephritis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786829010 Alport's syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786829010 Alport's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5257081000241111 néphrite chronique héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5257081000241111 néphrite chronique héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


17 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary nephritis Is a Hereditary disorder of the urinary system false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nephritis Is a Nephritis (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nephritis Associated morphology inflammation chronique false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary nephritis Finding site Glomerulus structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary nephritis Is a Chronic disease of genitourinary system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nephritis Is a Chronic inflammatory disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nephritis Course Chronic (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nephritis Is a Chronic glomerulonephritis false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nephritis Is a Glomerulonephritis true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nephritis Finding site Glomerulus structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary nephritis Associated morphology inflammation chronique false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary nephritis Is a Hereditary nephropathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nephritis Associated morphology Chronic inflammatory morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
syndrome d'Epstein Is a False Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Progressive hereditary glomerulonephritis without deafness Is a True Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Alport syndrome-like hereditary nephritis Is a False Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
syndrome de Fechtner Is a False Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Familial interstitial nephritis Is a True Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Other familial glomerulonephritis Is a False Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
[EDTA] Hereditary nephritis with nerve deafness (Alport's Syndrome) associated with renal failure Is a False Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary diffuse mesangial proliferative glomerulonephritis Is a False Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary diffuse mesangiocapillary glomerulonephritis Is a True Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary diffuse endocapillary proliferative glomerulonephritis (disorder) Is a True Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary diffuse membranous glomerulonephritis (disorder) Is a True Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type III Is a True Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Alport syndrome autosomal dominant Is a False Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Alport syndrome autosomal recessive Is a False Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Alport syndrome X-linked (disorder) Is a False Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder) Is a True Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Dyschondrosteose - Nephritis Is a False Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus, glomerulonephritis, marfanoid habitus syndrome (disorder) Is a True Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Alport syndrome (disorder) Is a True Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)
Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome Is a True Hereditary nephritis 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 True Hereditary nephritis Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start