Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Neurofaciodigitorenal syndrome |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Nephroscopy and biopsy of renal lesion (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Nephroscopy (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acute kidney injury due to trauma (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Unroofing of cyst of kidney |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Endoscopic de-roofing of multiple cysts of kidney (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Thyrocerebrorenal syndrome |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Acute kidney failure stage 1 (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Acute kidney failure stage 2 (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Acute kidney failure stage 3 (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Collecting duct carcinoma of kidney (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chromophobe renal cell carcinoma |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ischemic contracture of kidney |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Spastic paraplegia, nephritis, deafness syndrome |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Tubulocystic renal cell carcinoma (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Papillary renal cell carcinoma (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
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) |
1 |
Postpartum acute renal failure |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Specimen of fluid from cyst of kidney |
Specimen source topography |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Familial papillary thyroid carcinoma with renal papillary neoplasia syndrome (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Primary hyperoxaluria type III (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Irregularly contracted kidney |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Complex renal cyst (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ischemia of kidney (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Renal hypocalciuria (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Local destruction of lesion of kidney (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Local excision of lesion of kidney |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hydronephrosis due to calculus of kidney and ureter |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Nephropathy following pre-eclampsia (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Nephropathy following eclampsia (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Renal failure following molar pregnancy (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Multiple renal cysts (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Multiple acquired kidney cysts |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Multicystic renal dysplasia |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Renal coloboma syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Percutaneous needle biopsy of kidney using ultrasonographic guidance (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Percutaneous needle biopsy of kidney using ultrasonographic guidance (procedure) |
Procedure site - Indirect (attribute) |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Neonatal haemorrhage of kidney |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Renal hypersensitivity caused by drug |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Radionuclide imaging of kidney using technetium (99m-Tc) succimer |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
MiT family translocation renal cell carcinoma |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A rare subtype of renal cell carcinoma, occurring in the context of end-stage kidney disease and acquired cystic kidney disease, characterized by a usually well circumscribed, solid, multifocal, bilateral tumor with inter- or intracellular microlumen formation (leading to cribiform architecture). Tumors are often diagnosed incidentally in early stages, although complications caused by renal cysts (dull flank or abdominal pain, fever) or renal parenchymal bleeding may mask the underlying neoplastic process. Most have an indolent behavior. |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Mucinous tubular and spindle cell renal carcinoma |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Renal hepatic pancreatic dysplasia (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Radionuclide imaging of kidney using technetium (99m-Tc) pentavalent succimer for renal neoplasm |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal dominant polycystic kidney disease |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Radio-renal syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Acquired magnesium-losing nephropathy |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acquired complex renal cyst (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hydrocalycosis |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Acquired polycystic kidney disease (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acquired renal cystic disease (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Single acquired kidney cyst |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Peripelvic (lymphatic) cyst |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Radionuclide imaging of kidney using technetium (99m-Tc) pentetic acid (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Closed biopsy of kidney (procedure) |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Plasmodium malariae malaria with nephropathy |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Renal coccidiosis |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A rare syndromic intellectual disability characterised by early developmental delay with failure to thrive, intellectual disability, congenital hepatic fibrosis, renal cystic dysplasia, and dysmorphic facial features (bilateral ptosis, anteverted nostrils, high arched palate, and micrognathia). Variable additional features have been reported, including cerebellar anomalies, postaxial polydactyly, syndactyly, genital anomalies, tachypnoea. There have been no further descriptions in the literature since 1987. |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
An extremely rare developmental defect during embryogenesis malformation syndrome with congenital muscular torticollis associated with skin anomalies (such as multiple keloids, pigmented nevi, epithelioma), urogenital malformations (including cryptorchidism and hypospadias) and renal dysplasia (for example chronic pyelonephritis, renal atrophy). Additional reported features include varicose veins, intellectual disability and musculoskeletal anomalies. |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Syphilis of kidney |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Late syphilis of kidney |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Thymic, renal, anal, lung dysplasia syndrome |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
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 |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Faciocardiorenal syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary renal dysplasia (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Glycogenosis with glucoaminophosphaturia |
Finding site |
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) |
1 |
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Bilateral congenital primary hydronephrosis (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
15q overgrowth syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Oligomeganephronic hypoplasia of kidney |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Acrorenal mandibular syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Multinodular goiter, cystic kidney, polydactyly syndrome |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Renal dysplasia with limb defect syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Anomaly of fetal kidney (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Nephrocystin 3-related Meckel-like syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
MRI guided high intensity focused ultrasound ablation of lesion of kidney |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
MRI guided high intensity focused ultrasound ablation of lesion of kidney |
Procedure site - Direct (attribute) |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hypotonia cystinuria syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Atypical hypotonia cystinuria syndrome (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Ischemic contracture of kidney |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
IgA nephropathy |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Primary IgA nephropathy |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
IgA nephropathy associated with liver disease |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Familial immunoglobulin A nephropathy |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Bilateral congenital primary hydronephrosis (disorder) |
Finding site |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Laparoscopic transplant of kidney using robotic assistance |
Procedure site - Indirect (attribute) |
False |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Granulomatous sarcoid nephropathy |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Infected renal cyst |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Infectious disorder of kidney |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Infections of kidney in pregnancy |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Multicystic renal dysplasia |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Recurrent kidney stone (disorder) |
Finding site |
True |
Kidney structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |