Category:Kidney diseases
From WikiMD's Wellness Encyclopedia
 | This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes N00-N19, N20.0 should be included in this category. |
Pages in category "Kidney diseases"
The following 200 pages are in this category, out of 388 total.
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- AA amyloidosis
- Acquired cystic kidney disease-associated renal cell carcinoma
- Acute glomerulonephritis
- Acute interstitial nephritis
- Acute kidney failure
- Acute kidney injury
- Acute proliferative glomerulonephritis
- Acute renal failure
- Acute tubular necrosis
- Acute uric acid nephropathy
- Adenine phosphoribosyltransferase deficiency
- AGXT
- Albuminuria
- Allergic interstitial nephritis
- Alport
- Alport syndrome
- Aluminium toxicity in dialysis patients
- Aminoaciduria
- Analgesic nephropathy
- Anaritide
- Anti-glomerular basement membrane antibody
- APKD
- Apolipoprotein L1
- ARF
- Assessment of kidney function
- Atypical hemolytic uremic syndrome
- Autosomal dominant polycystic kidney
- Autosomal dominant polycystic kidney disease
- Autosomal dominant tubulointerstitial kidney disease due to REN mutations
- Autosomal recessive polycystic kidney
- Autosomal recessive polycystic kidney disease
B
- Balkan endemic nephropathy
- Balkan nephropathy
- Bartter's syndrome
- Batu
- Bellini duct carcinoma
- Benign nephrosclerosis
- Berger
- Bilateral renal agenesis dominant type
- Biliary malformation renal tubular insufficiency
- BK polyomavirus
- Blood urea nitrogen test
- Blunt kidney trauma
- Brachymesomelia renal syndrome
- Branchio-oto-renal syndrome
- Bright
- Bright's disease
- BSND
C
- C3 glomerulonephritis
- Cacchi–Ricci disease
- Calciphylaxis
- Cardiovascular–kidney–metabolic syndrome
- CFHR5 nephropathy
- Chromophobe renal carcinoma
- Chronic allograft nephropathy
- Chronic kidney failure
- Chronic pyelonephritis
- Chronic renal disease
- Chronic renal failure
- CLCN5
- Clear-cell sarcoma of the kidney
- CNTO-530
- COL4A4
- Complications of hypertension
- Congenital nephrotic syndrome
- Congenital nephrotic syndrome Finnish type
- Congenital urinary tract obstruction
- Contrast nephropathy
- Contrast-induced nephropathy
- Crescentic glomerulonephritis
- Crystal deposit disease
- Cylindruria
- Cystic kidney disease
- Cystic nephroma
- Cystinuria-lysinuria
D
- D-minus hemolytic uremic syndrome
- D-plus hemolytic uremic syndrome
- Dent disease
- Dent's disease
- Denys–Drash syndrome
- Diabetes insipidus, nephrogenic type 2
- Diabetes insipidus, nephrogenic type 3
- Diabetes insipidus, nephrogenic, recessive type
- Diabetic kidney disease
- Diabetic nephropathy
- Dialysis adequacy
- Dialysis disequilibrium syndrome
- Dibasic aminoaciduria type 1
- Diffuse leiomyomatosis with Alport syndrome
- Diffuse proliferative nephritis
- Dioctophymosis
- Distal primary acidosis, familial
- Distal renal tubular acidosis
- DMSA scan
- Drug-induced interstitial nephritis
E
F
G
- Galloway-Mowat syndrome
- Gitelman
- Gitelman syndrome
- Glomectomy
- Glomerular filtration rate
- Glomerular hyperfiltration
- Glomerulocystic kidney disease
- Glomerulonephritis
- Glomerulonephritis sparse hair telangiectases
- Glomerulonephrosis
- Glomerulopathy
- Glomerulosclerosis
- Glomus coccygeum
- Goldblatt–Wallis syndrome
- Goodpasture syndrome
- Gordon hyperkaliemia-hypertension syndrome
H
- Haemodialysis
- Haemodialysis-associated amyloidosis
- Haemolytic-uremic syndrome
- Hamburger disease
- Hantavirus hemorrhagic fever with renal syndrome
- Hemodialysis product
- Hemolytic Uremic Syndrome
- Hemolytic-uremic syndrome
- Hepatic fibrosis renal cysts mental retardation
- Hepatorenal syndrome
- Hereditary primary Fanconi disease
- Heredofamilial amyloidosis
- Heritable disease
- Histidinuria renal tubular defect syndrome
- HIV associated nephropathy
- HIV-associated nephropathy
- HOGA1
- Hydronephrosis
- Hydronephrosis peculiar facial expression
- Hydrothorax
- Hydroureter
- Hyperalbuminemia
- Hypercalcinuria macular coloboma
- Hyperchloremia
- Hyperchloremic acidosis
- Hypernephroma
- Hyperoxaluria type 2
- Hyperphosphatemia
- Hypertension, renovascular
- Hypertensive disorders
- Hypertensive hyperkalemia, familial
- Hypertensive nephropathy
- Hypertensive nephrosclerosis
- Hypokalemic alkalosis with hypercalcinuria
- Hyporeninemic hypoaldosteronism
- Hyposthenuria
- Hypouricemia
I
K
- Stage III transitional cell cancer of the renal pelvis and ureter
- Kidney disease
- Kidney dysplasia
- Kidney Failure
- Kidney infection
- Kidney ischemia
- Kidney paired donation
- Kidney stone
- Kidney stone disease
- Kidney stones
- Kidney Stones
- Kidney transplantation
- Kidney tumour
- Kimmelstiel-Wilson syndrome
- Kobret
L
M
- Magnesium defect in renal tubular transport of
- Medullary cystic disease
- Medullary cystic kidney disease
- Autosomal dominant tubulointerstitial kidney disease
- Autosomal dominant tubulointerstitial kidney disease due to MUC1 mutations
- Autosomal dominant tubulointerstitial kidney disease due to UMOD mutations
- Medullary sponge kidney
- Megalocytic interstitial nephritis
