Nephropathy

Kidney disease, or renal disease, also known as nephropathy, is damage to or disease of a kidney. Nephritis is an inflammatory kidney disease and has several types according to the location of the inflammation. [Source: Wikipedia ]

Synonyms
Renal insufficiency
May Cause
Hyperechoic renal parenchyma
May Be Caused by
Acute interstitial nephritis and uveitis syndrome
Adenine phosphoribosyltransferase deficiency
AIDS
Alagille syndrome
Alkaptonuria
Alport syndrome
Amelogenesis imperfecta - nephrocalcinosis
Amyloidosis
Asphyxiating thoracic dysplasia
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy
Bardet-Biedl syndrome
Bartter syndrome
Behçet disease
Bile nephrosis
Carbonic anhydrase II deficiency
Cataract - nephropathy - encephalopathy
Cockayne syndrome
Congenital AIDS
Cystinosis
Cystinuria
Diabetes mellitus
Ellis-van Creveld syndrome
Fabry disease
Familial hyperuricosuria
Familial Mediterranean fever
Fanconi syndrome
Galloway-Mowat syndrome
Gaucher disease
Gitelman syndrome
Glycogen storage disease type 1
Glycogen storage disease type 5
Goodpasture syndrome
Gout
Hemolytic-uremic syndrome
Hemophilia
Henoch-Schönlein purpura
Hepatic fibrosis-renal cystic disease
Hepatorenal syndrome
Hereditary endotheliopathy
Hutterite cerebro-osteonephrodysplasia
Hydrocephalus - blue sclerae - nephropathy
Hypervitaminosis D
Lesch-Nyhan syndrome
Lowe syndrome
Male pseudohermaphroditism
Nail-patella syndrome
Nephronophthisis
Nephropathy - deafness - hyperparathyroidism
Osteolysis with nephropathy
Oxalosis
Paraneoplastic syndrome
Polycystic kidneys and liver
Potter sequence
Prune-belly syndrome
Pseudohypoaldosteronism
Renal tubular acidosis
Riley-Day syndrome
Saldino-Mainzer syndrome
Senior-Loken syndrome
Sickle cell disease
Spondylometaphyseal dysplasia Sedaghatian type
Trichorhinophalangeal dysplasia type 1
Tyrosinemia
Wegener granulomatosis
Wilson disease
Wiskott-Aldrich syndrome
Wolcott-Rallison syndrome
Zellweger syndrome
Renal insufficiency
Acute interstitial nephritis and uveitis syndrome
Adenine phosphoribosyltransferase deficiency
AIDS
Alagille syndrome
Alkaptonuria
Alport syndrome
Amelogenesis imperfecta - nephrocalcinosis
Amyloidosis
Asphyxiating thoracic dysplasia
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy
Bardet-Biedl syndrome
Bartter syndrome
Behçet disease
Bile nephrosis
Carbonic anhydrase II deficiency
Cataract - nephropathy - encephalopathy
Cockayne syndrome
Congenital AIDS
Cystinosis
Cystinuria
Diabetes mellitus
Ellis-van Creveld syndrome
Fabry disease
Familial hyperuricosuria
Familial Mediterranean fever
Fanconi syndrome
Galloway-Mowat syndrome
Gaucher disease
Gitelman syndrome
Glycogen storage disease type 1
Glycogen storage disease type 5
Goodpasture syndrome
Gout
Hemolytic-uremic syndrome
Hemophilia
Henoch-Schönlein purpura
Hepatic fibrosis-renal cystic disease
Hepatorenal syndrome
Hereditary endotheliopathy
Hutterite cerebro-osteonephrodysplasia
Hydrocephalus - blue sclerae - nephropathy
Hypervitaminosis D
Lesch-Nyhan syndrome
Lowe syndrome
Male pseudohermaphroditism
Nail-patella syndrome
Nephronophthisis
Nephropathy - deafness - hyperparathyroidism
Osteolysis with nephropathy
Oxalosis
Paraneoplastic syndrome
Polycystic kidneys and liver
Potter sequence
Prune-belly syndrome
Pseudohypoaldosteronism
Renal tubular acidosis
Riley-Day syndrome
Saldino-Mainzer syndrome
Senior-Loken syndrome
Sickle cell disease
Spondylometaphyseal dysplasia Sedaghatian type
Trichorhinophalangeal dysplasia type 1
Tyrosinemia
Wegener granulomatosis
Wilson disease
Wiskott-Aldrich syndrome
Wolcott-Rallison syndrome
Zellweger syndrome