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29704000: Structure of parenchyma 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
49693017 Renal parenchyma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
49694011 Parenchyma of kidney en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484373017 Structure of parenchyma of kidney en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
760628013 Structure of parenchyma of kidney (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


99 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Structure of parenchyma of kidney Is a Kidney part true Inferred relationship Some
Structure of parenchyma of kidney partie de Entire kidney false Additional relationship Some
Structure of parenchyma of kidney Is a Organ parenchyma true Inferred relationship Some
Structure of parenchyma of kidney Laterality Side (qualifier value) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital Fanconi syndrome Finding site False Structure of parenchyma of kidney Inferred relationship Some 2
Congenital nephritis Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Mumps nephritis Finding site False Structure of parenchyma of kidney Inferred relationship Some 2
Bartter's syndrome with hypercalciuria and nephrocalcinosis Finding site False Structure of parenchyma of kidney Inferred relationship Some 3
Heavy metal nephropathy Finding site False Structure of parenchyma of kidney Inferred relationship Some 2
Acute nephritic syndrome, minor glomerular abnormality Finding site True Structure of parenchyma of kidney Inferred relationship Some 2
Balkan nephropathy Finding site False Structure of parenchyma of kidney Inferred relationship Some 2
Acute on chronic tubulointerstitial nephritis (disorder) Finding site False Structure of parenchyma of kidney Inferred relationship Some 1
Xanthogranulomatous pyelonephritis Finding site False Structure of parenchyma of kidney Inferred relationship Some 4
Idiopathic granulomatous interstitial nephropathy Finding site False Structure of parenchyma of kidney Inferred relationship Some 4
Acute nephritic syndrome co-occurrent and due to membranoproliferative glomerulonephritis type III Finding site True Structure of parenchyma of kidney Inferred relationship Some 3
Rapidly progressive nephritic syndrome co-occurrent and due to membranoproliferative glomerulonephritis type III Finding site True Structure of parenchyma of kidney Inferred relationship Some 5
A rare genetic disorder characterized by the association of complete or partial congenital aniridia (and associated eyes abnormalities), genitourinary anomalies (ranging from sexual ambiguity to ectopic testis), variable degrees of intellectual disability and an increased risk of developing Wilms tumors. A minority of patients develop kidney failure. Other variable findings may include obesity and duplicated halluces. Finding site False Structure of parenchyma of kidney Inferred relationship Some 3
Structure of parenchyma of right kidney (body structure) Is a True Structure of parenchyma of kidney Inferred relationship Some
Structure of parenchyma of left kidney (body structure) Is a True Structure of parenchyma of kidney Inferred relationship Some
Familial renal cell carcinoma (disorder) Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Bartter syndrome type 4a (disorder) Finding site False Structure of parenchyma of kidney Inferred relationship Some 3
Bacterial nephritis (disorder) Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Autosomal dominant tubulointerstitial disease Finding site False Structure of parenchyma of kidney Inferred relationship Some
Hereditary clear cell renal cell carcinoma (ccRCC) is a hereditary renal cancer syndrome defined as development of ccRCC in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other tumor predisposing syndromes associated with ccRCC, such as tuberous sclerosis or Birt-Hogg-Dubé syndrome. Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Chronic radiation nephritis Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
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. Finding site True Structure of parenchyma of kidney Inferred relationship Some 2
Disorder of renal parenchyma (disorder) Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Chronic tubulointerstitial nephritis caused by heavy metal Finding site False Structure of parenchyma of kidney Inferred relationship Some 1
Chronic mercury nephropathy Finding site False Structure of parenchyma of kidney Inferred relationship Some 1
Granulomatous tubulointerstitial nephritis (disorder) Finding site False Structure of parenchyma of kidney Inferred relationship Some 2
Structure of medulla of kidney Is a True Structure of parenchyma of kidney Inferred relationship Some
Structure of cortex of kidney Is a True Structure of parenchyma of kidney Inferred relationship Some
Chronic lead nephropathy (disorder) Finding site False Structure of parenchyma of kidney Inferred relationship Some 1
Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome is a rare, genetic, overgrowth syndrome characterized by global developmental delay, macrosomia with subsequent somatic overgrowth, bilateral cystic lung lesions, congenital nephromegaly and bilateral Wilms tumor. Craniofacial dysmorphism includes macrocephaly, frontal bossing, large anterior fontanelle, mild hypertelorism, ear pit, flat nasal bridge, anteverted nares and mild micrognathia. Additional features may include brain and skeletal anomalies, enlarged protuberant abdomen, fat pads on dorsum of feet and toes, and rugated soles with skin folds, as well as umbilical/inguinal hernia and autistic behavior. Finding site True Structure of parenchyma of kidney Inferred relationship Some 2
Saturnine nephropathy Finding site False Structure of parenchyma of kidney Inferred relationship Some 1
Chronic cadmium nephropathy Finding site False Structure of parenchyma of kidney Inferred relationship Some 1
Chronic infective interstitial nephritis Finding site False Structure of parenchyma 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 parenchyma of kidney Inferred relationship Some 2
Henoch-Schönlein nephritis Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Nephritis Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Radiation nephritis Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Acute radiation nephritis Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Xanthogranulomatous pyelonephritis Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Neoplasm of parenchyma of kidney (disorder) Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Papillary thyroid carcinoma with renal papillary neoplasia (disorder) Finding site False Structure of parenchyma of kidney Inferred relationship Some 1
Nephritis caused by drug (disorder) Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Complete disruption of kidney parenchyma with open wound into cavity Finding site True Structure of parenchyma of kidney Inferred relationship Some 2
Cystic partially differentiated nephroblastoma of kidney Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Compression of parenchyma of kidney Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Metastatic cystadenocarcinoma to kidney (disorder) Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Nephrotoxic serum nephritis Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Primary cystadenocarcinoma of kidney Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Primary papillary cystadenocarcinoma of kidney Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Metastatic papillary cystadenocarcinoma to kidney (disorder) Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Primary clear cell carcinoma of kidney Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Primary nephroblastoma (disorder) Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Nephrocalcinosis Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Tryptophan malabsorption syndrome Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Microscopic nephrocalcinosis Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Macroscopic nephrocalcinosis Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (FHHN) is a form of familial primary hypomagnesemia, characterized by recurrent urinary tract infections, nephrolithiasis, bilateral nephrocalcinosis, renal magnesium (Mg) wasting, hypercalciuria and kidney failure. Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Enamel-renal syndrome Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
A rare genetic disease characterized by the association of Fanconi syndrome and nephrocalcinosis in addition to neonatal hyperinsulinism and macrosomia. Patients display a phenotype of proximal tubulopathy characterized by generalized aminoaciduria, low molecular weight proteinuria, glycosuria, hyperphosphaturia and hypouricemia, and additional features not normally seen in Fanconi syndrome (apart from nephrocalcinosis), namely renal impairment, hypercalciuria with relative hypocalcemia, and hypermagnesemia. Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Oxalosis (disorder) Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Neonatal nephrocalcinosis Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis (disorder) Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) Finding site True Structure of parenchyma of kidney Inferred relationship Some 1
Diffuse hyperplastic perilobular nephroblastomatosis (disorder) Finding site True Structure of parenchyma of kidney Inferred relationship Some 2
Diffuse hyperplastic perilobular nephroblastomatosis (disorder) Finding site True Structure of parenchyma of kidney Inferred relationship Some 1

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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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