TubeTalk Pronunciation

How to pronounce “minimal change disease

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Pronunciation guide for minimal change disease

Learning goal
Practice the English pronunciation of minimal change disease with real speech in context.
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Definition summary
(pathology) A disease of the kidneys, characterized by proteinuria, edema, weight gain, and hypoalbuminaemia.

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A Deep Dive Into “minimal change disease

Meaning

  • [Noun]
  • (pathology) A disease of the kidneys, characterized by proteinuria, edema, weight gain, and hypoalbuminaemia.

Practice Nearby Words

diabetic nephropathy, kidney disease, nephrosis, nephritis, nephritic syndrome, nephrogenic diabetes insipidus, chronic kidney disease, renal tubular acidosis, focal segmental glomerulosclerosis, fanconi syndrome, interstitial nephritis, bright's disease, glomerulonephritis, glomerulonephrosis, lupus nephritis, nephropathy, kidney failure, iga nephropathy, glomerulonephropathy, nephrotic syndrome, acute tubular necrosis, hypertensive kidney disease, renal papillary necrosis, balkan endemic nephropathy, calciphylaxis, kidney stone disease, oligomeganephronia, gitelman syndrome, renal osteodystrophy, glomerulopathy, microangiopathy, polycystic kidney disease, medullary sponge kidney, fabry disease, congenital nephrotic syndrome, renal artery stenosis, goodpasture syndrome, membranous glomerulonephritis, systemic vasculitis, polyarteritis nodosa, nephronophthisis, nephrocalcinosis, tubulopathy, nephropyelitis, hemorrhagic cystitis, glomerulosclerosis, cystopyelonephritis, algodystrophy, niemann-pick disease, granulomatosis with polyangiitis, hepatorenal syndrome, chronic liver disease, pyruvate dehydrogenase deficiency, acute kidney injury, proximal renal tubular acidosis, neurogenic bladder dysfunction, kidney cancer, lesch-nyhan syndrome, microscopic polyangiitis, leigh syndrome, chronic granulomatous disease, adrenoleukodystrophy, nephrolithiasis, gaucher's disease, cystinuria, glycogen storage disease type v, myotonic dystrophy, renal vein thrombosis, autoimmune hepatitis, lymphocytic colitis, cystathioninuria, muscular dystrophy, iminoglycinuria, fibromuscular dysplasia, congenital myasthenic syndrome, peripheral neuropathy, multicystic dysplastic kidney, agranulocytosis, heart failure, congestive heart failure, motor neuron disease, methylmalonic acidemia, myelodysplastic syndrome, refsum's disease, granulocytopenia, small fiber peripheral neuropathy, ischemic colitis, tyrosinemia type i, progressive muscular atrophy, lateral medullary syndrome, neurodegenerative disease, bartter syndrome, hashimoto's thyroiditis, pure red cell aplasia, glycogen storage disease type ii, cerebral vasculitis, central diabetes insipidus, glycogen storage disease type i, chyluria, non-alcoholic fatty liver disease

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