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Acute glomerulonephritis, IgA nephropathy (N00.801) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Acute glomerulonephritis with proliferative glomerulonephritis (N00.800x004) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is bein
Acute nephritis with necrotizing glomerulonephritis lesion (N00.800x001) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being co
Acute nephritic syndrome, other (N00.800) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Acute nephritic syndrome with diffuse crescentic glomerulonephritis (N00.700) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is bei
Acute nephritic syndrome with dense deposit disease (N00.600) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Acute nephritic syndrome with diffuse mesangiocapillary glomerulonephritis (N00.500) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction
Acute nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis (N00.400) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological in
Acute mesangioproliferative glomerulonephritis (N00.301) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Acute nephritic syndrome with diffuse mesangioproliferative glomerulonephritis (N00.300) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduc
Acute nephritic syndrome with diffuse membranous glomerulonephritis (N00.200) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is bei
Focal necrotizing glomerulonephritis (N00.100x001) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Acute nephritic syndrome with focal and segmental glomerular lesion (N00.100) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is bei
Acute nephritic syndrome with minor glomerular abnormality (N00.000) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compil
Lupus nephritis is renal involvement of SLE; glucocorticoids + mycophenolate/cyclophosphamide; hydroxychloroquine; BP/proteinuria control; follow-up nephrology/rheumatology.
肾内科Renovascular hypertension is high BP from renal-artery stenosis (atherosclerosis/FMD): treat by ACEi/ARB, renal angioplasty/stenting, surgery.
肾内科Renal amyloidosis is amyloid deposition in kidney: nephrotic-range proteinuria, progressive renal failure; AL (primary) or AA (secondary); treat underlying cause, chemotherapy/transplant.
肾内科Fabry disease is X-linked alpha-galactosidase-A deficiency causing globotriaosylceramide accumulation: acroparesthesias, angiokeratoma, hypohidrosis, renal/cardiac/cerebrovascular disease; enzyme replacement therapy.
肾内科Fanconi syndrome is proximal-tubular defect causing glycosuria, phosphaturia, aminoaciduria, bicarbonate/waste salt loss: rickets, acidosis, dehydration; inherited (cystinosis) or acquired; replace electrolytes/bicarbonate.
肾内科Bartter syndrome is inherited loop-of-Henle salt-wasting tubulopathy: hypokalemic metabolic alkalosis, hyperreninemic hyperaldosteronism, normal BP, hypercalciuria; presents in childhood with failure to thrive.
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