Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Renal washings (specimen) |
Specimen source topography |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Light chain nephropathy due to multiple myeloma (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Tuberculosis of kidney |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
néphropathie tuberculeuse |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
End stage renal disease due to hypertension |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Acute kidney injury caused by contrast agent (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Morphologic change of kidney due to chronic nephritic syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Chronic kidney disease mineral and bone disorder |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Renal impairment caused by Polyomavirus (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Disorder of kidney co-occurrent with human immunodeficiency virus infection (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
néoplasme carcinoïde malin du rein |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Renal failure syndrome co-occurrent with human immunodeficiency virus infection (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Nephropathy caused by BK polyomavirus (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic kidney disease stage 5 on dialysis (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Chronic kidney disease stage 5 with transplant (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Anaemia co-occurrent and due to chronic kidney disease stage 3 |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
A rare familial renal cancer syndrome characterized by a predisposition for developing bilateral and multifocal classic type papillary renal cell carcinomas (formerly known as type 1 papillary renal cell carcinoma until the 2022 WHO classification of renal tumors). |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Renal dysplasia co-occurrent with megalocystis and sirenomelia |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Doppler ultrasonography of kidney |
Procedure site - Direct (attribute) |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Fibulo-ulnar hypoplasia and renal anomalies syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Familial papillary thyroid carcinoma with renal papillary neoplasia syndrome (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare rodent-borne, potentially severe, haemorrhagic disease caused by Old World Hantaviruses characterised by high fever, malaise, headache, myalgia, arthralgia, backache, abdominal pain, oliguria/renal failure and systemic haemorrhagic manifestations. |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Percutaneous irreversible electroporation ablation of neoplasm of kidney using computed tomography guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Percutaneous irreversible electroporation ablation of neoplasm of kidney using computed tomography guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Malakoplakia of kidney |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Joubert syndrome with renal defect |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
néphrose coocurrente avec et due au lupus érythémateux systémique |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Single photon emission computed tomography of kidney using dimercaptosuccinic acid (procedure) |
Procedure site - Direct (attribute) |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Single photon emission computed tomography using dimercaptosuccinic acid with computed tomography of kidney with contrast (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Single photon emission computed tomography using dimercaptosuccinic acid with computed tomography of kidney with contrast (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Transplantation of kidney and pancreas (procedure) |
Procedure site - Indirect (attribute) |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Insertion of fiducial marker into kidney using computed tomography guidance (procedure) |
Procedure site - Indirect (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Insertion of fiducial marker into kidney using computed tomography guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Renal dysplasia with limb defect syndrome (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Pyelonephritis due to kidney stone (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Chronic pyelonephritis |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Chronic pyelonephritis without medullary necrosis |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Familial non-obstructive reflux-associated chronic pyelonephritis |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Fungal infection of kidney |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Renal candidiasis (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Papillary thyroid carcinoma with renal papillary neoplasia (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Renal cell carcinoma of kidney except renal pelvis (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary renal dysplasia (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Secondary renal dysplasia (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital hemorrhagic renal cyst (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Bilateral medullary sponge kidney (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Bilateral medullary sponge kidney (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Bilateral multicystic renal dysplasia (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Bilateral congenital primary hydronephrosis (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Aristolochic acid nephropathy |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dent disease type 1 (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dent disease type 2 (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Bartter syndrome type 4a (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Acrorenal mandibular syndrome (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Acrorenal syndrome |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare, severe, circulatory system disease characterised by premature, diffuse, severe atherosclerosis (including the aorta and renal, coronary, and cerebral arteries), sensorineural deafness, diabetes mellitus, progressive neurological deterioration with cerebellar symptoms and photomyoclonic seizures, and progressive nephropathy. Partial deficiency of mitochondrial complexes III and IV in the kidney and fibroblasts (but not in muscle) may be associated. There have been no further descriptions in the literature since 1994. |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare syndrome of multiple congenital anomalies characterized by radial ray malformations, renal abnormalities (mild malrotation, ectopia, horseshoe kidney, renal hypoplasia, vesico-ureteral reflux, bladder diverticula), and ophthalmological abnormalities (mainly colobomas, but also microphthalmia, ptosis, and Duane anomaly). The phenotype overlaps with other SALL4-related disorders including Okihiro syndrome and Holt-Oram syndrome. |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
néoplasme carcinoïde malin du rein |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Cyst of kidney (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acute kidney injury due to hypovolemia (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Acute kidney injury due to circulatory failure (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Acute kidney injury due to sepsis (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Single photon emission computed tomography of kidney (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
syndrome d'Okamoto |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Chronic kidney disease following donor nephrectomy (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Chronic kidney disease due to and following excision of neoplasm of kidney (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Chronic kidney disease due to systemic infection |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Excision of neoplasm of kidney (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic kidney disease due to traumatic loss of kidney (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Distal renal tubular acidosis co-occurrent with sensorineural deafness |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Perlman syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare congenital urogenital anomaly characterised by the presence of double uterus (didelphys, bicornuate or septum-complete or partial), unilateral cervico-vaginal obstruction (obstructed hemivagina-communicant, not communicant or septate and unilateral cervical atresia) and ipsilateral renal anomalies (renal agenesis and/or other urinary tract anomalies). Patients are usually diagnosed at puberty after menarche due to recurrent severe dysmenorrhoea, chronic pelvic pain, excessive foul smelling mucopurulent discharge, spotting and intermenstrual bleeding (depending on the existence of uterine or vaginal communications). Fever, dyspareunia, and a palpable abdominal, pelvic or vaginal mass (mucocolpos or pyocolpos) may also be present. |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Perlman syndrome (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Juvenile cataract, microcornea, renal glucosuria syndrome |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Percutaneous biopsy of kidney using computed tomography guidance (procedure) |
Procedure site - Indirect (attribute) |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Percutaneous biopsy of kidney using computed tomography guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Familial haemolytic uraemic syndrome |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Percutaneous needle biopsy of kidney using fluoroscopic guidance (procedure) |
Procedure site - Indirect (attribute) |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Percutaneous needle biopsy of kidney using fluoroscopic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Renal insufficiency (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Acute renal insufficiency (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Chronic renal insufficiency (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Juvenile cataract, microcornea, renal glucosuria syndrome |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Glomerulopathy with fibronectin deposits 2 (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Faciocardiorenal syndrome (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Bilateral medullary sponge kidney (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Multinodular goiter, cystic kidney, polydactyly syndrome |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Thymic, renal, anal, lung dysplasia syndrome |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
SERKAL syndrome |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
SERKAL syndrome |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Magnetic resonance imaging of kidney without contrast (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
CT of kidney-ureter-bladder without contrast |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A rare monoclonal gammopathy characterized by renal proximal tubule dysfunction secondary to monoclonal kappa light chain deposits in proximal tubular cells. Clinical presentation is with variable chronic kidney disease, low molecular weight proteinuria, aminoaciduria, hyperphosphaturia, uricosuria, bicarbonaturia, and non-diabetic glycosuria. Renal phosphate and urate wasting may cause hypophosphatemia and hypouricemia. |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Puncture of cyst of kidney using ultrasonographic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hypoparathyroidism, deafness, renal disease syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
11 |
Gestational proteinuria without hypertension (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Neurofaciodigitorenal syndrome |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Neurofaciodigitorenal syndrome |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |