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276585000: Congenital nephritis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2004. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
412798014 Congenital nephritis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
669517010 Congenital nephritis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5853421000241119 néphrite congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital nephritis Is a Congenital anomaly of the kidney (disorder) false Inferred relationship Some
Congenital nephritis Is a Newborn renal dysfunction false Inferred relationship Some
Congenital nephritis Occurrence Neonatal false Inferred relationship Some
Congenital nephritis Finding site Kidney structure false Inferred relationship Some 1
Congenital nephritis Finding site Urinary tract includes entire kidney and the urinary tract proper which relate to the ureter, bladder and urethra. false Inferred relationship Some 9
Congenital nephritis Occurrence Congenital false Inferred relationship Some
Congenital nephritis Course Multiple superficial injuries of lower leg false Inferred relationship Some
Congenital nephritis Associated morphology anomalie congénitale false Inferred relationship Some 2
Congenital nephritis Finding site Kidney structure false Inferred relationship Some 2
Congenital nephritis Is a Inflammation of specific body organs false Inferred relationship Some
Congenital nephritis Is a Inflammatory disorder of genitourinary system (disorder) false Inferred relationship Some
Congenital nephritis Associated morphology inflammation false Inferred relationship Some 1
Congenital nephritis Finding site Kidney structure false Inferred relationship Some 1
Congenital nephritis Finding site Kidney structure false Inferred relationship Some 2
Congenital nephritis Finding site Kidney structure false Inferred relationship Some 1
Congenital nephritis Finding site Kidney structure false Inferred relationship Some 2
Congenital nephritis Finding site Kidney structure false Inferred relationship Some 1
Congenital nephritis Finding site Kidney structure false Inferred relationship Some 2
Congenital nephritis Finding site Kidney structure false Inferred relationship Some 1
Congenital nephritis Finding site Kidney structure false Inferred relationship Some 2
Congenital nephritis Finding site Kidney structure false Inferred relationship Some 1
Congenital nephritis Finding site Kidney structure false Inferred relationship Some 2
Congenital nephritis Occurrence Congenital true Inferred relationship Some 1
Congenital nephritis Finding site Kidney structure false Inferred relationship Some 3
Congenital nephritis Is a Congenital disease true Inferred relationship Some
Congenital nephritis Is a Kidney disease false Inferred relationship Some
Congenital nephritis Associated morphology inflammation false Inferred relationship Some 1
Congenital nephritis Is a Nephritis true Inferred relationship Some
Congenital nephritis Finding site Structure of parenchyma of kidney true Inferred relationship Some 1
Congenital nephritis Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial mesangial sclerosis Is a False Congenital nephritis 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 Congenital nephritis Inferred relationship Some
syndrome de dyschondrostéose - néphropathie Is a False Congenital nephritis Inferred relationship Some
A rare renal disease characterized by the association of X-linked Alport syndrome (glomerular nephropathy, sensorineural deafness and ocular anomalies) and benign proliferation of visceral smooth muscle cells along the gastrointestinal, respiratory, and female genital tracts and clinically manifests with dysphagia, dyspnea, cough, stridor, postprandial vomiting, retrosternal or epigastric pain, recurrent pneumonia, and clitoral hypertrophy in females. Is a True Congenital nephritis 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 Congenital nephritis Inferred relationship Some
Lowe-Kohn-Cohen syndrome is an extremely rare anorectal malformation syndrome characterized by imperforate anus, closed ano-perineal fistula, preauricular skin tag and absent renal abnormalities and pre-axial limb deformities. There have been no further descriptions in the literature since 1983. Is a True Congenital nephritis Inferred relationship Some

Reference Sets

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