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Autosomal Recessive Polycystic Kidney Disease
Autosomal recessive polycystic kidney disease
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Kidney diseases
(89)
Autosomal dominant polycystic kidney disease
End Stage Renal Disease (US Federal Program)
End-stage kidney disease
Glomerulonephritis
Kidney stones
Kidney stones
Medullary cystic kidney disease
Multicystic dysplastic kidney
Polycystic kidney disease
Renal agenesis
Renal artery obstruction
Renal disease
Uremia
Wilms tumor
Abderhalde- n-Kaufmann-Lignac syndrome
Acute kidney injury
Acute proliferative glomerulonephritis
Adenine phosphorib- osyltransferase deficiency
Alport syndrome
Aminoaciduria
Analgesic nephropathy
Azotemia
Bardoxolone methyl
Bellini duct carcinoma
Benign nephrosclerosis
Bright's disease
Cardiorenal syndrome
Clear-cell sarcoma of the kidney
Congenital nephrotic syndrome
Conorenal syndrome
Cystic nephroma
Danubian endemic familial nephropathy
Deaths from kidney disease
Dent's disease
Diabetic nephropathy
Diffuse proliferative nephritis
EAST syndrome
Exner syndrome
Fanconi syndrome
Fibromuscular dysplasia
Focal proliferative nephritis
Focal segmental glomerulosclerosis
Galloway Mowat syndrome
Gitelman syndrome
Glycosuria
Goodpasture's syndrome
HIV-associated nephropathy
Horseshoe kidney
Hypercalcaemia
Hypertensive nephropathy
Hyponephrosis
Hypophosphatemia
IgA nephropathy
Interstitial nephritis
Juxtaglomerular cell tumor
Kidney Research UK
Kidney cancer
Kidney stone formers
Kidney tumour
Lloyd's sign
Lupus nephritis
Metanephric adenoma
Milk-alkali syndrome
Minimal change disease
Minimal mesangial glomerulonephritis
Nephritis
Nephromegaly
Nephroptosis
Nephrotic syndrome
Nutcracker syndrome
Oncocytoma
Papillorenal syndrome
Phoslo
Phosphate nephropathy
Pyonephrosis
Rapidly progressive glomerulonephritis
Rebound diuresis
Renal cell carcinoma
Renal medullary carcinoma
Renal oncocytoma
Renal osteodystrophy
Renal papillary necrosis
Renal tubular acidosis
Renal vein thrombosis
Secondary hypertension
Shunt nephritis
Sickle cell nephropathy
Tetracapsuloides bryosalmonae
Thin basement membrane disease
Wunderlich syndrome
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Genetic disorders
(15)
Congenital hepatic fibrosis
Caroli syndrome
Polycystic liver disease
Nephronophthisis
Ciliopathy
Ciliopathy
Meckel syndrome
Inherited disease
Polydactyly
Loken Senior syndrome
Tuberous sclerosis
Dandy-Walker malformation
Huntington disease
Polycystic kidney disease
Autosomal dominant polycystic kidney disease
Medullary cystic kidney disease
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Congenital disorders
Potter sequence
Pulmonary hypoplasia
Genetic disorders
Multicystic dysplastic kidney
Polydactyly
Loken Senior syndrome
Dandy-Walker malformation
Nephrology
(105)
Blood in the urine
Dialysis
Home dialysis
Kidney development
Kidney failure
Kidney failure
Kidney transplantation
Peritoneal dialysis
Proteinuria
Pyelonephritis
Renal ectopia
Renal replacement therapy
Urinary tract infections
Acid-base disturbances
Acute tubular necrosis
Acute uric acid nephropathy
Albuminuria
Anuria
Artificial kidney
BUN-to-creatinine ratio
Bartter syndrome
Bladder augmentation
Blood urea nitrogen
Branchio-oto-renal syndrome
Calciphylaxis
Cholesterol embolism
Clearance (medicine)
Crush syndrome
Cystatin C
DRIL
Diabetes insipidus
Dialysis disequilibrium syndrome
Diuresis
End Stage Renal Disease (US Federal Program)
End-stage kidney disease
Erythropoi- esis-stimulating agents
Forced diuresis
Geriatric nephrology
Haff disease
Hemofiltration
Hemolytic-uremic syndrome
Henoch–Schönlein purpura
Hepatorenal syndrome
Hormones of the kidneys
Hugh R. Brady
Hydronephrosis
Hyperkalemia
Hypermagnesemia
Hypertension
Hypokalemia
Hypomagnesemia
Hypomagnesemia with secondary hypocalcemia
Hyponephrosis
Icodextrin
Iminoglycinuria
Immersion diuresis
International Society of Nephrology
Isosthenuria
Kidney diseases
Kidney organizations
Loin pain hematuria syndrome
MILLER banding
March hematuria
Meckel syndrome
Membranopr- oliferative glomerulonephritis
Microalbuminuria
Microangiopathic hemolytic anemia
Nephritic syndrome
Nephrogenic diabetes insipidus
Nephrogenic systemic fibrosis
Nephrologists
Nephrotoxicity
Normal anion gap acidosis
Orellanine
Osmotic diuresis
Osmotic nephrosis
Percutaneous nephrolithotomy
Percutaneous nephrostomy
Peritoneal equilibration test
Phosphate binders
Plasma renin activity
Potter sequence
Pseudohypo- aldosteronism
Pump leak model
Reference ranges for urine tests
Reflux nephropathy
Renal Association
Renal clearance ratio
Renal colic
Renal dialysis
Renal segmental hypoplasia
Renal threshold
Renovascular hypertension
Rhabdomyolysis
Richard Bright (physician)
Serum osmotic gap
Sevelamer
Supernumerary kidney
Systemic lupus erythematosus
Tram tracking
Urinalysis
Urinary cast
Uroscopy
Vascular access steal syndrome
Vesicouretic reflux
Wegener's granulomatosis
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Urinary system
Renal
Congenital cystic dysplasia
Renal medulla
Polycystic kidney disease
Nephronophthisis
Medullary cystic kidney disease
Gastroenterology
Portal hypertension
Choledochal cysts
Hepatolithiasis
Congenital hepatic fibrosis
Caroli syndrome
Dominance (genetics)
Autosomal dominant
Recessive
Dominance (genetics) (Co-dominance)
Dominance (genetics) (Codominance)
Dominance (genetics) (Dominant Negative)
Dominance (genetics) (Incomplete dominance)
Hepatology
Intrahepatic bile ducts
Cholangiocarcinoma
Caroli syndrome
Portal hypertension
Meckel syndrome
Hepatolithiasis
Obstetrics
Oligohydramnios
Prenatal diagnosis
Ultrasound imaging
Amniotic fluid
Pulmonary hypoplasia
Symptoms
Cysts
Flank pain
Pain in the back
Excessive urination at night
Blood in the urine
Uremia
Diseases and disorders
(35)
Cystic kidney disease
Polycystic kidney disease infantile type
Arima syndrome
Cholangitis
Cacchi-Ricci disease
Cacchi-Ricci disease
Juvenile nephronophthisis
Aneurysms
Senior loken syndrome
Kidney diseases
Congenital hepatic fibrosis
Caroli syndrome
Polycystic liver disease
Portal hypertension
Medullary cystic kidney disease
Oligohydramnios
End-stage kidney disease
Potter sequence
Multicystic dysplastic kidney
Renal artery obstruction
Blood in the urine
Polydactyly
Wilms tumor
Proteinuria
Pyelonephritis
Tuberous sclerosis
Aplasia
Urinary system
Uremia
Choledochal cysts
Renal agenesis
Glomerulonephritis
Hepatolithiasis
Huntington disease
Kidney stones
Urinary tract infections
more...
See also
(20)
Diseases and disorders
ARPKD
PKHD1
ADPKD
PKD1
PKD1
PKD2 (gene)
Anatomy
Vasodilation
Kidney disorder
Medicine
IFT88
Renal dysplasia
Cilium
Nephron
Autosomal
Renal function
Intraflagellar transport
Alport
Mutation analysis
J. Pediatr.
more...
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