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 |