List of MeSH codes (C12)
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.
MeSH C12 – urologic and male genital diseases
MeSH C12.294.365 – infertility
- MeSH C12.294.365.700 – infertility, male
- MeSH C12.294.365.700.508 – oligospermia
MeSH C12.294.644 – sexual dysfunction, physiological
- MeSH C12.294.644.486 – impotence
- MeSH C12.294.644.486.500 – impotence, vasculogenic
MeSH C12.740.700 – urogenital abnormalities
- MeSH C12.740.700.132 – bladder exstrophy
- MeSH C12.740.700.258 – cryptorchidism
- MeSH C12.740.700.374 – epispadias
- MeSH C12.740.700.445 – frasier syndrome
- MeSH C12.740.700.516 – hypospadias
- MeSH C12.740.700.629 – multicystic dysplastic kidney
- MeSH C12.740.700.742 – nephritis, hereditary
- MeSH C12.740.700.842 – sex differentiation disorders
- MeSH C12.740.700.842.309 – gonadal dysgenesis
- MeSH C12.740.700.842.309.195 – gonadal dysgenesis, 46,xx
- MeSH C12.740.700.842.309.293 – gonadal dysgenesis, 46,xy
- MeSH C12.740.700.842.309.391 – gonadal dysgenesis, mixed
- MeSH C12.740.700.842.309.695 – turner syndrome
- MeSH C12.740.700.842.316 – hermaphroditism
- MeSH C12.740.700.842.316.313 – hermaphroditism, true
- MeSH C12.740.700.842.316.627 – pseudohermaphroditism
- MeSH C12.740.700.842.316.627.109 – androgen-insensitivity syndrome
- MeSH C12.740.700.842.316.627.220 – denys-drash syndrome
- MeSH C12.740.700.842.425 – kallmann syndrome
- MeSH C12.740.700.842.454 – klinefelter syndrome
- MeSH C12.740.700.921 – wagr syndrome
MeSH C12.740.800 – urogenital neoplasms
- MeSH C12.740.800.410 – genital neoplasms, male
- MeSH C12.740.800.410.600 – penile neoplasms
- MeSH C12.740.800.410.650 – prostatic neoplasms
- MeSH C12.740.800.410.875 – testicular neoplasms
- MeSH C12.740.800.820 – urologic neoplasms
- MeSH C12.740.800.820.125 – bladder neoplasms
- MeSH C12.740.800.820.750 – kidney neoplasms
- MeSH C12.740.800.820.750.160 – carcinoma, renal cell
- MeSH C12.740.800.820.750.585 – wilms tumor
- MeSH C12.740.800.820.750.585.220 – denys-drash syndrome
- MeSH C12.740.800.820.750.585.950 – wagr syndrome
- MeSH C12.740.800.820.750.790 – nephroma, mesoblastic
- MeSH C12.740.800.820.875 – ureteral neoplasms
- MeSH C12.740.800.820.937 – urethral neoplasms
MeSH C12.777.103 – bladder diseases
- MeSH C12.777.103.124 – bladder calculi
- MeSH C12.777.103.132 – bladder exstrophy
- MeSH C12.777.103.187 – bladder fistula
- MeSH C12.777.103.187.733 – vesicovaginal fistula
- MeSH C12.777.103.249 – bladder neck obstruction
- MeSH C12.777.103.312 – bladder neoplasms
- MeSH C12.777.103.374 – bladder, neurogenic
- MeSH C12.777.103.495 – cystitis
- MeSH C12.777.103.495.500 – cystitis, interstitial
- MeSH C12.777.103.920 – vesico-ureteral reflux
MeSH C12.777.419 – kidney diseases
- MeSH C12.777.419.050 – aids-associated nephropathy
- MeSH C12.777.419.078 – anuria
- MeSH C12.777.419.135 – diabetes insipidus
- MeSH C12.777.419.135.500 – diabetes insipidus, nephrogenic
- MeSH C12.777.419.135.750 – diabetes insipidus, neurogenic
- MeSH C12.777.419.135.875 – wolfram syndrome
- MeSH C12.777.419.192 – diabetic nephropathies
- MeSH C12.777.419.250 – fanconi syndrome
- MeSH C12.777.419.291 – hepatorenal syndrome
- MeSH C12.777.419.307 – hydronephrosis
- MeSH C12.777.419.320 – hyperoxaluria, primary
- MeSH C12.777.419.331 – hypertension, renal
- MeSH C12.777.419.331.490 – hypertension, renovascular
- MeSH C12.777.419.373 – kidney calculi
- MeSH C12.777.419.393 – kidney cortex necrosis
- MeSH C12.777.419.403 – kidney diseases, cystic
- MeSH C12.777.419.403.500 – medullary sponge kidney
- MeSH C12.777.419.403.750 – multicystic dysplastic kidney
- MeSH C12.777.419.403.875 – polycystic kidney diseases
- MeSH C12.777.419.403.875.500 – polycystic kidney, autosomal dominant
- MeSH C12.777.419.403.875.510 – polycystic kidney, autosomal recessive
- MeSH C12.777.419.473 – kidney neoplasms
- MeSH C12.777.419.473.160 – carcinoma, renal cell
- MeSH C12.777.419.473.585 – wilms tumor
- MeSH C12.777.419.473.585.220 – denys-drash syndrome
- MeSH C12.777.419.473.585.950 – wagr syndrome
- MeSH C12.777.419.473.790 – nephroma, mesoblastic
- MeSH C12.777.419.493 – kidney papillary necrosis
- MeSH C12.777.419.570 – nephritis
- MeSH C12.777.419.570.363 – glomerulonephritis
- MeSH C12.777.419.570.363.304 – anti-glomerular basement membrane disease
- MeSH C12.777.419.570.363.304.300 – goodpasture syndrome
- MeSH C12.777.419.570.363.608 – glomerulonephritis, iga
- MeSH C12.777.419.570.363.615 – glomerulonephritis, membranoproliferative
- MeSH C12.777.419.570.363.625 – glomerulonephritis, membranous
- MeSH C12.777.419.570.363.640 – glomerulosclerosis, focal
- MeSH C12.777.419.570.363.680 – lupus nephritis
- MeSH C12.777.419.570.620 – nephritis, hereditary
- MeSH C12.777.419.570.643 – nephritis, interstitial
- MeSH C12.777.419.570.643.150 – balkan nephropathy
- MeSH C12.777.419.570.643.790 – pyelonephritis
- MeSH C12.777.419.570.643.790.810 – pyelonephritis, xanthogranulomatous
- MeSH C12.777.419.590 – nephrocalcinosis
- MeSH C12.777.419.610 – nephrosclerosis
- MeSH C12.777.419.630 – nephrosis
- MeSH C12.777.419.630.477 – nephrosis, lipoid
- MeSH C12.777.419.630.643 – nephrotic syndrome
- MeSH C12.777.419.685 – perinephritis
- MeSH C12.777.419.744 – pyelitis
- MeSH C12.777.419.744.717 – pyelonephritis
- MeSH C12.777.419.744.717.810 – pyelonephritis, xanthogranulomatous
- MeSH C12.777.419.775 – renal artery obstruction
- MeSH C12.777.419.780 – renal insufficiency
- MeSH C12.777.419.780.500 – kidney failure
- MeSH C12.777.419.780.500.205 – kidney failure, acute
- MeSH C12.777.419.780.500.205.500 – kidney tubular necrosis, acute
- MeSH C12.777.419.780.500.602 – kidney failure, chronic
- MeSH C12.777.419.780.625 – renal insufficiency, acute
- MeSH C12.777.419.780.625.500 – kidney failure, acute
- MeSH C12.777.419.780.625.500.400 – kidney tubular necrosis, acute
- MeSH C12.777.419.780.750 – renal insufficiency, chronic
- MeSH C12.777.419.780.750.500 – kidney failure, chronic
- MeSH C12.777.419.795 – renal osteodystrophy
- MeSH C12.777.419.815 – renal tubular transport, inborn errors
- MeSH C12.777.419.815.093 – acidosis, renal tubular
- MeSH C12.777.419.815.191 – aminoaciduria, renal
- MeSH C12.777.419.815.191.250 – cystinuria
- MeSH C12.777.419.815.191.457 – hartnup disease
- MeSH C12.777.419.815.279 – bartter syndrome
- MeSH C12.777.419.815.368 – cystinosis
- MeSH C12.777.419.815.368.210 – fanconi syndrome
- MeSH C12.777.419.815.532 – glycosuria, renal
- MeSH C12.777.419.815.647 – hypophosphatemia, familial
- MeSH C12.777.419.815.720 – oculocerebrorenal syndrome
- MeSH C12.777.419.815.770 – pseudohypoaldosteronism
- MeSH C12.777.419.912 – tuberculosis, renal
- MeSH C12.777.419.936 – uremia
- MeSH C12.777.419.936.463 – hemolytic-uremic syndrome
- MeSH C12.777.419.978 – zellweger syndrome
MeSH C12.777.725 – ureteral diseases
- MeSH C12.777.725.576 – ureteral calculi
- MeSH C12.777.725.676 – ureteral neoplasms
- MeSH C12.777.725.776 – ureteral obstruction
- MeSH C12.777.725.876 – ureterocele
MeSH C12.777.809 – urinary calculi
- MeSH C12.777.809.186 – bladder calculi
- MeSH C12.777.809.503 – kidney calculi
- MeSH C12.777.809.851 – ureteral calculi
MeSH C12.777.850 – urinary fistula
- MeSH C12.777.850.312 – bladder fistula
- MeSH C12.777.850.312.733 – vesicovaginal fistula
MeSH C12.777.934 – urination disorders
- MeSH C12.777.934.284 – enuresis
- MeSH C12.777.934.600 – oliguria
- MeSH C12.777.934.600.078 – anuria
- MeSH C12.777.934.616 – polyuria
- MeSH C12.777.934.852 – urinary incontinence
- MeSH C12.777.934.852.727 – urinary incontinence, stress
- MeSH C12.777.934.880 – urinary retention
The list continues at List of MeSH codes (C13).
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