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1. N00. Acute nephritic syndrome
2. N01. Rapidly progressive nephritic syndrome
3. N02. Recurrent and persistent haematuria
4. N03. Chronic nephritic syndrome
5. N04. Nephrotic syndrome
6. N05. Unspecified nephritic syndrome
7. N06. Isolated proteinuria with specified morphological lesion
8. N07. Hereditary nephropathy, not elsewhere classified
9. N08*. Glomerular disorders in diseases classified elsewhere

Use additional code, if desired, to identify external cause (Chapter XX) or presence of renal failure (N17-N19).
Excludes: hypertensive renal disease (I12.-)

The following fourth-character subdivisions classify morphological changes and are for use with categories N00-N07. Subdivisions .0-.8 should not normally be used unless these have been specifically identified (e.g. by renal biopsy or autopsy). The three-character categories relate to clinical syndromes.

.0  Minor glomerular abnormality
Minimal change lesion

.1  Focal and segmental glomerular lesions
Focal and segmental:
. hyalinosis
. sclerosis
Focal glomerulonephritis

.2  Diffuse membranous glomerulonephritis

.3  Diffuse mesangial proliferative glomerulonephritis

.4  Diffuse endocapillary proliferative glomerulonephritis

.5  Diffuse mesangiocapillary glomerulonephritis
Membranoproliferative glomerulonephritis, types 1 and 3, or NOS

.6  Dense deposit disease
Membranoproliferative glomerulonephritis, type 2

.7  Diffuse crescentic glomerulonephritis
Extracapillary glomerulonephritis
  
.8  Other
Proliferative glomerulonephritis NOS

.9  Unspecified




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