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50235001: Structure of interstitial tissue of kidney (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
83679015 Interstitial tissue of kidney en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
495623018 Structure of interstitial tissue of kidney en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
788001012 Structure of interstitial tissue of kidney (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Structure of interstitial tissue of kidney Is a Interstitial tissue true Inferred relationship Some
Structure of interstitial tissue of kidney Is a Abdominopelvic soft tissue structure false Inferred relationship Some
Structure of interstitial tissue of kidney Is a Kidney part true Inferred relationship Some
Structure of interstitial tissue of kidney partie de Entire kidney false Additional relationship Some
Structure of interstitial tissue of kidney Is a Connective tissue by site false Inferred relationship Some
Structure of interstitial tissue of kidney Is a Soft tissue of abdomen false Inferred relationship Some
Structure of interstitial tissue of kidney Laterality Side (qualifier value) true Inferred relationship Some
Structure of interstitial tissue of kidney Is a Structure of soft tissue within abdominopelvic cavity (body structure) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Acute tubulointerstitial nephritis associated with systemic infection Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 3
Acute bacterial tubulointerstitial nephritis Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 4
Tubulointerstitial nephropathy due to Sjogren syndrome (disorder) Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 3
Acute fungal tubulointerstitial nephritis Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 2
Acute viral tubulointerstitial nephritis (disorder) Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 2
Bartter syndrome type 4a (disorder) Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 5
Autosomal dominant tubulointerstitial disease Finding site False Structure of interstitial tissue of kidney Inferred relationship Some
Renal interstitial fibrosis Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
A rare, genetic renal disease characterized by slowly progressive, chronic, tubulointerstitial nephritis, leading to end-stage renal disease before the age of 50 years, manifesting with mild proteinuria, glucosuria and, occasionally, urinary sediment abnormalities (mainly hematuria). Mild extrarenal manifestations, such as recurrent upper respiratory tract infections and abnormal liver function tests, may be associated. Renal biopsy reveals severe, chronic, interstitial fibrosis and tubular changes, as well as hallmark karyomegalic tubular epithelial cells which line the proximal and distal tubules and have enlarged, hyperchromatic nuclei. Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 3
Chronic tubulointerstitial nephritis caused by heavy metal Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 2
Chronic mercury nephropathy Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 2
Chronic lead nephropathy (disorder) Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 2
Saturnine nephropathy Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 2
Chronic cadmium nephropathy Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 2
Chronic infective interstitial nephritis Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 2
A rare, genetic renal disease characterized by slowly progressive, chronic, tubulointerstitial nephritis, leading to end-stage renal disease before the age of 50 years, manifesting with mild proteinuria, glucosuria and, occasionally, urinary sediment abnormalities (mainly hematuria). Mild extrarenal manifestations, such as recurrent upper respiratory tract infections and abnormal liver function tests, may be associated. Renal biopsy reveals severe, chronic, interstitial fibrosis and tubular changes, as well as hallmark karyomegalic tubular epithelial cells which line the proximal and distal tubules and have enlarged, hyperchromatic nuclei. Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Primary tubulointerstitial nephritis (disorder) Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Diphtheria tubulointerstitial nephropathy Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Bartter's syndrome with hypercalciuria and nephrocalcinosis Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 1
Tubulointerstitial nephropathy due to Sjogren syndrome (disorder) Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 2
Drug-induced tubulointerstitial nephritis (disorder) Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Heavy-metal-induced tubulointerstitial nephritis (disorder) Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Bartter syndrome (disorder) Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 1
tubulopathie familiale avec hypokaliémie et hypomagnésémie Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 1
A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Secondary tubulointerstitial nephritis (disorder) Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Bartter syndrome type 3 (disorder) Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 1
Epilepsy, ataxia, sensorineural deafness, and tubulopathy syndrome Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 1
Bartter syndrome type 4a (disorder) Finding site False Structure of interstitial tissue of kidney Inferred relationship Some 1
Acute tubulo-interstitial nephritis due to immunological disorder Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Chronic tubulointerstitial nephritis following renal transplantation (disorder) Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Chronic tubulo-interstitial nephritis due to connective tissue disorder Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Chronic tubulointerstitial nephritis due to ischaemia Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Chronic tubulointerstitial nephritis due to neoplastic disease (disorder) Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Chronic tubulointerstitial nephritis due to metabolic disease (disorder) Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
A rare renal disease occurring in the setting of a systemic IgG4 related disease (IgG4-RD). The disorder is characterized by a fibrosing tubulointerstitial nephritis consisting of predominantly IgG4+ plasma cells with/without glomerulonephritis, retroperitoneal fibrosis and hydronephrosis. Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Renal tubulo-interstitial disorder due to cystinosis (disorder) Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
Acute on chronic tubulointerstitial nephritis (disorder) Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 1
A rare, genetic renal disease characterized by slowly progressive, chronic, tubulointerstitial nephritis, leading to end-stage renal disease before the age of 50 years, manifesting with mild proteinuria, glucosuria and, occasionally, urinary sediment abnormalities (mainly hematuria). Mild extrarenal manifestations, such as recurrent upper respiratory tract infections and abnormal liver function tests, may be associated. Renal biopsy reveals severe, chronic, interstitial fibrosis and tubular changes, as well as hallmark karyomegalic tubular epithelial cells which line the proximal and distal tubules and have enlarged, hyperchromatic nuclei. Finding site True Structure of interstitial tissue of kidney Inferred relationship Some 2

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Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

Anatomy structure and entire association reference set (foundation metadata concept)

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