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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
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 (disorder) Is a Hereditary disorder of the urinary system false Inferred relationship Some
Hereditary nephritis (disorder) Is a Nephritis false Inferred relationship Some
Hereditary nephritis (disorder) Associated morphology inflammation chronique false Inferred relationship Some 1
Hereditary nephritis (disorder) Finding site Glomerulus structure false Inferred relationship Some 1
Hereditary nephritis (disorder) Is a Chronic disease of genitourinary system false Inferred relationship Some
Hereditary nephritis (disorder) Is a Chronic inflammatory disorder false Inferred relationship Some
Hereditary nephritis (disorder) Course Chronic false Inferred relationship Some
Hereditary nephritis (disorder) Is a Chronic glomerulonephritis false Inferred relationship Some
Hereditary nephritis (disorder) Is a Glomerulonephritis true Inferred relationship Some
Hereditary nephritis (disorder) Finding site Glomerulus structure true Inferred relationship Some 1
Hereditary nephritis (disorder) Associated morphology inflammation chronique false Inferred relationship Some 1
Hereditary nephritis (disorder) Is a Hereditary nephropathy (disorder) true Inferred relationship Some
Hereditary nephritis (disorder) Associated morphology Chronic inflammatory morphology (morphologic abnormality) true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
syndrome d'Epstein Is a False Hereditary nephritis (disorder) Inferred relationship Some
Progressive hereditary glomerulonephritis without deafness Is a True Hereditary nephritis (disorder) Inferred relationship Some
Alport syndrome-like hereditary nephritis Is a False Hereditary nephritis (disorder) Inferred relationship Some
syndrome de Fechtner Is a False Hereditary nephritis (disorder) Inferred relationship Some
Familial interstitial nephritis Is a True Hereditary nephritis (disorder) Inferred relationship Some
Other familial glomerulonephritis Is a False Hereditary nephritis (disorder) Inferred relationship Some
[EDTA] Hereditary nephritis with nerve deafness (Alport's Syndrome) associated with renal failure Is a False Hereditary nephritis (disorder) Inferred relationship Some
Hereditary diffuse mesangial proliferative glomerulonephritis Is a False Hereditary nephritis (disorder) Inferred relationship Some
Hereditary diffuse mesangiocapillary glomerulonephritis Is a True Hereditary nephritis (disorder) Inferred relationship Some
Hereditary diffuse endocapillary proliferative glomerulonephritis (disorder) Is a True Hereditary nephritis (disorder) Inferred relationship Some
Hereditary diffuse membranous glomerulonephritis (disorder) Is a True Hereditary nephritis (disorder) Inferred relationship Some
Hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type III (disorder) Is a True Hereditary nephritis (disorder) Inferred relationship Some
Alport syndrome autosomal dominant (disorder) Is a False Hereditary nephritis (disorder) Inferred relationship Some
Alport syndrome autosomal recessive (disorder) Is a False Hereditary nephritis (disorder) Inferred relationship Some
Alport syndrome X-linked (disorder) Is a False Hereditary nephritis (disorder) Inferred relationship Some
A rare constitutional hemolytic anemia that is characterized by the association of Alport syndrome, midface hypoplasia, intellectual deficit and elliptocytosis. It has been described in two families. The syndrome is transmitted as an X-linked trait is caused by a contiguous gene deletion in Xq22.3 involving several genes including COL4A5, FACL4 and AMMECR1. Is a True Hereditary nephritis (disorder) Inferred relationship Some
syndrome de dyschondrostéose - néphropathie Is a False Hereditary nephritis (disorder) Inferred relationship Some
A rare intellectual disability syndrome characterized by intellectual deficit, marfanoid habitus, microcephaly, and glomerulonephritis. There have been no further reports since 1992. Is a True Hereditary nephritis (disorder) Inferred relationship Some
A rare renal disease characterized by glomerular nephropathy with hematuria progressing to end-stage renal disease (ESRD), frequently associated with sensorineural deafness, and occasionally with ocular anomalies. Is a True Hereditary nephritis (disorder) Inferred relationship Some
A rare, genetic, renal disease characterized by hereditary nephritis leading to nephrotic syndrome and end-stage renal failure associated with sensorineural hearing loss and pretibial skin blistering followed by atrophy. Other reported manifestations include bilateral lacrimal duct stenosis, dystrophic teeth and nails, bilateral cervical ribs, unilateral kidney, distal vaginal agenesis and anemia due to beta-thalassemia minor. Is a True Hereditary nephritis (disorder) 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 True Hereditary nephritis (disorder) Inferred relationship Some

This concept is not in any reference sets

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