List of MeSH codes (C12) explained
The following is a partial list of the "C" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM).
This list continues the information at List of MeSH codes (C11). Codes following these are found at List of MeSH codes (C13). For other MeSH codes, see List of MeSH codes.
The source for this content is the set of 2006 MeSH Trees from the NLM.
– urologic and male genital diseases
– genital diseases, male
– infertility
– penile diseases
– prostatic diseases
– sexual dysfunction, physiological
- – impotence
- – impotence, vasculogenic
– testicular diseases
– tuberculosis, urogenital
– tuberculosis, renal
– urogenital diseases
– urogenital abnormalities
– urologic diseases
- – aids-associated nephropathy
- – anuria
- – diabetes insipidus
- – diabetes insipidus, nephrogenic
- – diabetes insipidus, neurogenic
- – wolfram syndrome
- – diabetic nephropathies
- – fanconi syndrome
- – hepatorenal syndrome
- – hydronephrosis
- – hyperoxaluria, primary
- – hypertension, renal
- – hypertension, renovascular
- – kidney calculi
- – kidney cortex necrosis
- – kidney diseases, cystic
- – medullary sponge kidney
- – multicystic dysplastic kidney
- – polycystic kidney diseases
- – polycystic kidney, autosomal dominant
- – polycystic kidney, autosomal recessive
- – kidney neoplasms
- – carcinoma, renal cell
- – wilms tumor
- – denys-drash syndrome
- – wagr syndrome
- – nephroma, mesoblastic
- – kidney papillary necrosis
- – nephritis
- – glomerulonephritis
- – anti-glomerular basement membrane disease
- – goodpasture syndrome
- – glomerulonephritis, iga
- – glomerulonephritis, membranoproliferative
- – glomerulonephritis, membranous
- – glomerulosclerosis, focal
- – lupus nephritis
- – nephritis, hereditary
- – nephritis, interstitial
- – balkan nephropathy
- – pyelonephritis
- – pyelonephritis, xanthogranulomatous
- – nephrocalcinosis
- – nephrosclerosis
- – nephrosis
- – nephrosis, lipoid
- – nephrotic syndrome
- – perinephritis
- – pyelitis
- – pyelonephritis
- – pyelonephritis, xanthogranulomatous
- – renal artery obstruction
- – renal insufficiency
- – kidney failure
- – kidney failure, acute
- – kidney tubular necrosis, acute
- – kidney failure, chronic
- – renal insufficiency, acute
- – kidney failure, acute
- – kidney tubular necrosis, acute
- – renal insufficiency, chronic
- – kidney failure, chronic
- – renal osteodystrophy
- – renal tubular transport, inborn errors
- – acidosis, renal tubular
- – aminoaciduria, renal
- – cystinuria
- – hartnup disease
- – bartter syndrome
- – cystinosis
- – fanconi syndrome
- – glycosuria, renal
- – hypophosphatemia, familial
- – oculocerebrorenal syndrome
- – pseudohypoaldosteronism
- – tuberculosis, renal
- – uremia
- – hemolytic-uremic syndrome
- – zellweger syndrome
- – ureteral calculi
- – ureteral neoplasms
- – ureteral obstruction
- – ureterocele
– urethral diseases
– urinary tract infections
– urination disorders
----The list continues at List of MeSH codes (C13).