Glomerulonephritis and Nephrotic Syndrome (1489)    NLM VALUE SETS (802.2)

Name Value
NAME Glomerulonephritis and Nephrotic Syndrome
OID 2.16.840.1.113883.3.464.1003.109.12.1018
SHORT ID GANS18
VERSION DATE 2017-01-06 00:00:00
CODE LIST
  • CODES:
    • CODE DESCRIPTION:   
      Necrotizing glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Chronic glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome, focal and segmental glomerular 
      lesions (disorder)
      
    • CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome, diffuse membranous glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome, diffuse mesangial proliferative 
      glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome, diffuse endocapillary proliferative 
      glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome, diffuse mesangiocapillary glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome, dense deposit disease (disorder)
      
    • CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome, diffuse crescentic glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Recurrent and persistent hematuria, minor glomerular abnormality (disorder)
      
    • CODE DESCRIPTION:   
      Recurrent and persistent hematuria, focal and segmental glomerular lesions 
      (disorder)
      
    • CODE DESCRIPTION:   
      Recurrent and persistent hematuria, diffuse membranous glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Glomerulitis (disorder)
      
    • CODE DESCRIPTION:   
      Recurrent and persistent hematuria, diffuse mesangial proliferative glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Recurrent and persistent hematuria, diffuse endocapillary proliferative 
      glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Recurrent and persistent hematuria, diffuse mesangiocapillary glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Recurrent and persistent hematuria, dense deposit disease (disorder)
      
    • CODE DESCRIPTION:   
      Recurrent and persistent hematuria, diffuse crescentic glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Chronic nephritic syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Chronic nephritic syndrome, minor glomerular abnormality (disorder)
      
    • CODE DESCRIPTION:   
      Chronic nephritic syndrome, focal and segmental glomerular lesions (disorder)
      
    • CODE DESCRIPTION:   
      Chronic nephritic syndrome, diffuse endocapillary proliferative glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Chronic nephritic syndrome, diffuse mesangiocapillary glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Proximal renal tubular acidosis (disorder)
      
    • CODE DESCRIPTION:   
      Chronic nephritic syndrome, dense deposit disease (disorder)
      
    • CODE DESCRIPTION:   
      Chronic nephritic syndrome, diffuse crescentic glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Isolated proteinuria with specified morphological lesion (finding)
      
    • CODE DESCRIPTION:   
      Isolated proteinuria with specified morphological lesion, minor glomerular 
      abnormality (finding)
      
    • CODE DESCRIPTION:   
      Isolated proteinuria with specified morphological lesion, focal and segmental 
      glomerular lesions (finding)
      
    • CODE DESCRIPTION:   
      Isolated proteinuria with specified morphological lesion, diffuse membranous 
      glomerulonephritis (finding)
      
    • CODE DESCRIPTION:   
      Isolated proteinuria with specified morphological lesion, diffuse mesangial 
      proliferative glomerulonephritis (finding)
      
    • CODE DESCRIPTION:   
      Isolated proteinuria with specified morphological lesion, diffuse endocapillary 
      proliferative glomerulonephritis (finding)
      
    • CODE DESCRIPTION:   
      Isolated proteinuria with specified morphological lesion, diffuse mesangiocapillary 
      glomerulonephritis (finding)
      
    • CODE DESCRIPTION:   
      Isolated proteinuria with specified morphological lesion, dense deposit 
      disease (finding)
      
    • CODE DESCRIPTION:   
      Focal glomerular sclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Isolated proteinuria with specified morphological lesion, diffuse concentric 
      glomerulonephritis (finding)
      
    • CODE DESCRIPTION:   
      Glomerular disorders in neoplastic diseases (disorder)
      
    • CODE DESCRIPTION:   
      Glomerular disorders in blood diseases and disorders involving the immune 
      mechanism (disorder)
      
    • CODE DESCRIPTION:   
      Epstein syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Steroid-sensitive nephrotic syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Steroid-resistant nephrotic syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Steroid-dependent nephrotic syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Familial mesangial sclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Congenital nephrotic syndrome with focal glomerulosclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Drash syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Mesangial proliferative glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Bright's disease (disorder)
      
    • CODE DESCRIPTION:   
      Rapidly progressive glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Endocapillary glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Idiopathic endocapillary glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Post-infectious glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Post-infectious glomerulonephritis - Garland variety (disorder)
      
    • CODE DESCRIPTION:   
      Crescentic glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Steroid-sensitive minimal change glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Steroid-resistant minimal change glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Steroid-dependent minimal change glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Ischemic glomerulopathy (disorder)
      
    • CODE DESCRIPTION:   
      Focal segmental glomerulosclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Classical focal segmental glomerulosclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Hyperfiltration focal segmental glomerulosclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Immunoglobulin A nephropathy (disorder)
      
    • CODE DESCRIPTION:   
      Mesangiocapillary glomerulonephritis type III (disorder)
      
    • CODE DESCRIPTION:   
      Mesangiocapillary glomerulonephritis type IV (disorder)
      
    • CODE DESCRIPTION:   
      Immunoglobulin M nephropathy (disorder)
      
    • CODE DESCRIPTION:   
      C1q nephropathy (disorder)
      
    • CODE DESCRIPTION:   
      Membranous glomerulonephritis - stage I (disorder)
      
    • CODE DESCRIPTION:   
      Shunt nephritis (disorder)
      
    • CODE DESCRIPTION:   
      Membranous glomerulonephritis - stage II (disorder)
      
    • CODE DESCRIPTION:   
      Membranous glomerulonephritis - stage III (disorder)
      
    • CODE DESCRIPTION:   
      Membranous glomerulonephritis - stage IV (disorder)
      
    • CODE DESCRIPTION:   
      Membranous glomerulonephritis stage V (disorder)
      
    • CODE DESCRIPTION:   
      Thin basement membrane disease (disorder)
      
    • CODE DESCRIPTION:   
      Progressive hereditary glomerulonephritis without deafness (disorder)
      
    • CODE DESCRIPTION:   
      Alport syndrome-like hereditary nephritis (disorder)
      
    • CODE DESCRIPTION:   
      Fechtner syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Structural and functional abnormalities of the kidney (disorder)
      
    • CODE DESCRIPTION:   
      Familial proximal renal tubular acidosis (disorder)
      
    • CODE DESCRIPTION:   
      Diffuse type diabetic glomerulosclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Distal renal tubular acidosis (disorder)
      
    • CODE DESCRIPTION:   
      Hyperkalemic renal tubular acidosis (disorder)
      
    • CODE DESCRIPTION:   
      Magnesium-losing nephropathy (disorder)
      
    • CODE DESCRIPTION:   
      Inherited magnesium-losing nephropathy (disorder)
      
    • CODE DESCRIPTION:   
      Malignancy-associated glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Familial lobular glomerulopathy (disorder)
      
    • CODE DESCRIPTION:   
      Glomerulopathy with giant fibrillar deposits (disorder)
      
    • CODE DESCRIPTION:   
      Transplant glomerulopathy (disorder)
      
    • CODE DESCRIPTION:   
      Transplant glomerulopathy - early form (disorder)
      
    • CODE DESCRIPTION:   
      Transplant glomerulopathy - late form (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic-nephritic syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Cytomegalovirus-induced glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Primary pauci-immune necrotizing and crescentic glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Familial hypoplastic, glomerulocystic kidney (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome with minimal change glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Congenital nephritis (disorder)
      
    • CODE DESCRIPTION:   
      Immunoglobulin A nephropathy associated with liver disease (disorder)
      
    • CODE DESCRIPTION:   
      Diabetic glomerulopathy (disorder)
      
    • CODE DESCRIPTION:   
      Idiopathic crescentic glomerulonephritis, type II (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome secondary to systemic disease (disorder)
      
    • CODE DESCRIPTION:   
      Protein-losing nephropathy (disorder)
      
    • CODE DESCRIPTION:   
      Minimal change disease (disorder)
      
    • CODE DESCRIPTION:   
      Non-progressive hereditary glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Hereditary nephritis (disorder)
      
    • CODE DESCRIPTION:   
      Sarcoidosis with glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Diabetic glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Proliferative glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Autosomal dominant focal segmental glomerulosclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Idiopathic rapidly progressive glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Autosomal recessive focal segmental glomerulosclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Familial immunoglobulin A nephropathy (disorder)
      
    • CODE DESCRIPTION:   
      Lipoprotein glomerulopathy (disorder)
      
    • CODE DESCRIPTION:   
      Renal tubular acidosis (disorder)
      
    • CODE DESCRIPTION:   
      Congenital nephrotic syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Hyperkalemic distal renal tubular acidosis (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Nephritis (disorder)
      
    • CODE DESCRIPTION:   
      Diabetes-nephrosis syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Hypokalemic nephropathy (disorder)
      
    • CODE DESCRIPTION:   
      Idiopathic crescentic glomerulonephritis, type III (disorder)
      
    • CODE DESCRIPTION:   
      Acute benign hemorrhagic glomerulonephritic syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Acute nephropathy (disorder)
      
    • CODE DESCRIPTION:   
      Mesangiocapillary glomerulonephritis, type II (disorder)
      
    • CODE DESCRIPTION:   
      Diffuse endocapillary proliferative glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Hereditary nephrogenic diabetes insipidus (disorder)
      
    • CODE DESCRIPTION:   
      Acute nephritis (disorder)
      
    • CODE DESCRIPTION:   
      Benign arteriolar nephrosclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Nodular type diabetic glomerulosclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Idiopathic crescentic glomerulonephritis, type I (disorder)
      
    • CODE DESCRIPTION:   
      Diffuse crescentic glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Acute post-streptococcal glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Primary immunoglobulin A nephropathy (disorder)
      
    • CODE DESCRIPTION:   
      Fibrillary glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Mesangiocapillary glomerulonephritis, type I (disorder)
      
    • CODE DESCRIPTION:   
      Renal tubular defect (disorder)
      
    • CODE DESCRIPTION:   
      Membranous glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Mesangiocapillary glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Malignant arteriolar nephrosclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Acquired nephrogenic diabetes insipidus (disorder)
      
    • CODE DESCRIPTION:   
      Focal AND segmental proliferative glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Hypokalemic distal renal tubular acidosis (disorder)
      
    • CODE DESCRIPTION:   
      Arteriolar nephrosclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Armanni-Ebstein kidney (disorder)
      
    • CODE DESCRIPTION:   
      Nephrogenic diabetes insipidus (disorder)
      
    • CODE DESCRIPTION:   
      Drug-induced nephrogenic diabetes insipidus (disorder)
      
    • CODE DESCRIPTION:   
      Nephritic syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Subacute glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Healed glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Immune-complex glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Nephritis, nephrosis and nephrotic syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Acute proliferative glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Acute nephritis with lesions of necrotizing glomerulitis (disorder)
      
    • CODE DESCRIPTION:   
      Acute glomerulonephritis associated with another disorder (disorder)
      
    • CODE DESCRIPTION:   
      Acute focal nephritis (disorder)
      
    • CODE DESCRIPTION:   
      Acute diffuse nephritis (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome with proliferative glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Focal embolic nephritis syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome with membranous glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome with membranoproliferative glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome, minor glomerular abnormality (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome, focal and segmental glomerular lesions (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome, diffuse membranous glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome, diffuse mesangial proliferative glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome, diffuse endocapillary proliferative glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome, diffuse mesangiocapillary glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome, dense deposit disease (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome, diffuse crescentic glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Sclerosing glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Finnish congenital nephrotic syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome associated with another disorder (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome due to diabetes mellitus (disorder)
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome in polyarteritis nodosa (disorder)
      
    • CODE DESCRIPTION:   
      Chronic mesangial proliferative glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Chronic rapidly progressive glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Chronic glomerulonephritis associated with another disorder (disorder)
      
    • CODE DESCRIPTION:   
      Chronic exudative glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Chronic focal glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Chronic diffuse glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Renal osteodystrophy (disorder)
      
    • CODE DESCRIPTION:   
      Focal membranoproliferative glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Focal glomerulonephritis with focal recurrent macroscopic glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Anaphylactoid glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Berger's immunoglobulin A or immunoglobulin G nephropathy (disorder)
      
    • CODE DESCRIPTION:   
      Glomerulosclerosis (disorder)
      
    • CODE DESCRIPTION:   
      Impaired renal function disorder (disorder)
      
    • CODE DESCRIPTION:   
      Phosphate-losing tubular disorders (disorder)
      
    • CODE DESCRIPTION:   
      Albright's renal tubular acidosis (disorder)
      
    • CODE DESCRIPTION:   
      Renal function impairment with growth failure (disorder)
      
    • CODE DESCRIPTION:   
      Glomerular disease (disorder)
      
    • CODE DESCRIPTION:   
      Acute glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Acute nephritic syndrome, minor glomerular abnormality (disorder)
      
    • CODE DESCRIPTION:   
      Acute nephritic syndrome, focal and segmental glomerular lesions (disorder)
      
    • CODE DESCRIPTION:   
      Acute nephritic syndrome, diffuse membranous glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Acute nephritic syndrome, diffuse mesangial proliferative glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Acute nephritic syndrome, diffuse endocapillary proliferative glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Acute nephritic syndrome, diffuse mesangiocapillary glomerulonephritis 
      (disorder)
      
    • CODE DESCRIPTION:   
      Acute nephritic syndrome, dense deposit disease (disorder)
      
    • CODE DESCRIPTION:   
      Acute nephritic syndrome, diffuse crescentic glomerulonephritis (disorder)
      
    • CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome (disorder)
      
    • CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome, minor glomerular abnormality (disorder)
      
  • CODES:
    • CODE DESCRIPTION:   
      Acute glomerulonephritis with lesion of rapidly progressive glomerulonephritis
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome with unspecified pathological lesion in kidney
      
    • CODE DESCRIPTION:   
      Chronic glomerulonephritis with lesion of membranous glomerulonephritis
      
    • CODE DESCRIPTION:   
      Chronic glomerulonephritis with lesion of membranoproliferative glomerulonephritis
      
    • CODE DESCRIPTION:   
      Chronic glomerulonephritis with lesion of rapidly progressive glomerulonephritis
      
    • CODE DESCRIPTION:   
      Chronic glomerulonephritis in diseases classified elsewhere
      
    • CODE DESCRIPTION:   
      Chronic glomerulonephritis with other specified pathological lesion in kidney
      
    • CODE DESCRIPTION:   
      Chronic glomerulonephritis with unspecified pathological lesion in kidney
      
    • CODE DESCRIPTION:   
      Nephritis and nephropathy, not specified as acute or chronic, with lesion 
      of membranous glomerulonephritis
      
    • CODE DESCRIPTION:   
      Nephritis and nephropathy, not specified as acute or chronic, with lesion 
      of membranoproliferative glomerulonephritis
      
    • CODE DESCRIPTION:   
      Nephritis and nephropathy, not specified as acute or chronic, with lesion 
      of rapidly progressive glomerulonephritis
      
    • CODE DESCRIPTION:   
      Acute glomerulonephritis in diseases classified elsewhere
      
    • CODE DESCRIPTION:   
      Nephritis and nephropathy, not specified as acute or chronic, with lesion 
      of renal cortical necrosis
      
    • CODE DESCRIPTION:   
      Nephritis and nephropathy, not specified as acute or chronic, with lesion 
      of renal medullary necrosis
      
    • CODE DESCRIPTION:   
      Nephritis and nephropathy, not specified as acute or chronic, in diseases 
      classified elsewhere
      
    • CODE DESCRIPTION:   
      Nephritis and nephropathy, not specified as acute or chronic, with other 
      specified pathological lesion in kidney
      
    • CODE DESCRIPTION:   
      Nephritis and nephropathy, not specified as acute or chronic, with unspecified 
      pathological lesion in kidney
      
    • CODE DESCRIPTION:   
      Nephrogenic diabetes insipidus
      
    • CODE DESCRIPTION:   
      Secondary hyperparathyroidism (of renal origin)
      
    • CODE DESCRIPTION:   
      Other specified disorders resulting from impaired renal function
      
    • CODE DESCRIPTION:   
      Unspecified disorder resulting from impaired renal function
      
    • CODE:   581.0
      CODE DESCRIPTION:   
      Nephrotic syndrome with lesion of proliferative glomerulonephritis
      
    • CODE DESCRIPTION:   
      Acute glomerulonephritis with other specified pathological lesion in kidney
      
    • CODE:   582.0
      CODE DESCRIPTION:   
      Chronic glomerulonephritis with lesion of proliferative glomerulonephritis
      
    • CODE:   583.0
      CODE DESCRIPTION:   
      Nephritis and nephropathy, not specified as acute or chronic, with lesion 
      of proliferative glomerulonephritis
      
    • CODE:   588.0
      CODE DESCRIPTION:   
      Renal osteodystrophy
      
    • CODE DESCRIPTION:   
      Acute glomerulonephritis with unspecified pathological lesion in kidney
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome with lesion of membranous glomerulonephritis
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome with lesion of membranoproliferative glomerulonephritis
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome with lesion of minimal change glomerulonephritis
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome in diseases classified elsewhere
      
    • CODE DESCRIPTION:   
      Nephrotic syndrome with other specified pathological lesion in kidney
      
  • CODES:
    • CODE:   N00.0
      CODE DESCRIPTION:   
      Acute nephritic syndrome with minor glomerular abnormality
      
    • CODE:   N00.9
      CODE DESCRIPTION:   
      Acute nephritic syndrome with unspecified morphologic changes
      
    • CODE:   N01.0
      CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome with minor glomerular abnormality
      
    • CODE:   N01.1
      CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome with focal and segmental glomerular 
      lesions
      
    • CODE:   N01.2
      CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome with diffuse membranous glomerulonephritis
      
    • CODE:   N01.3
      CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome with diffuse mesangial proliferative 
      glomerulonephritis
      
    • CODE:   N01.4
      CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome with diffuse endocapillary proliferative 
      glomerulonephritis
      
    • CODE:   N01.5
      CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome with diffuse mesangiocapillary glomerulonephritis
      
    • CODE:   N01.6
      CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome with dense deposit disease
      
    • CODE:   N01.7
      CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome with diffuse crescentic glomerulonephritis
      
    • CODE:   N01.8
      CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome with other morphologic changes
      
    • CODE:   N00.1
      CODE DESCRIPTION:   
      Acute nephritic syndrome with focal and segmental glomerular lesions
      
    • CODE:   N01.9
      CODE DESCRIPTION:   
      Rapidly progressive nephritic syndrome with unspecified morphologic changes
      
    • CODE:   N02.0
      CODE DESCRIPTION:   
      Recurrent and persistent hematuria with minor glomerular abnormality
      
    • CODE:   N02.1
      CODE DESCRIPTION:   
      Recurrent and persistent hematuria with focal and segmental glomerular lesions
      
    • CODE:   N02.2
      CODE DESCRIPTION:   
      Recurrent and persistent hematuria with diffuse membranous glomerulonephritis
      
    • CODE:   N02.3
      CODE DESCRIPTION:   
      Recurrent and persistent hematuria with diffuse mesangial proliferative 
      glomerulonephritis
      
    • CODE:   N02.4
      CODE DESCRIPTION:   
      Recurrent and persistent hematuria with diffuse endocapillary proliferative 
      glomerulonephritis
      
    • CODE:   N02.5
      CODE DESCRIPTION:   
      Recurrent and persistent hematuria with diffuse mesangiocapillary glomerulonephritis
      
    • CODE:   N02.6
      CODE DESCRIPTION:   
      Recurrent and persistent hematuria with dense deposit disease
      
    • CODE:   N02.7
      CODE DESCRIPTION:   
      Recurrent and persistent hematuria with diffuse crescentic glomerulonephritis
      
    • CODE:   N02.8
      CODE DESCRIPTION:   
      Recurrent and persistent hematuria with other morphologic changes
      
    • CODE:   N00.2
      CODE DESCRIPTION:   
      Acute nephritic syndrome with diffuse membranous glomerulonephritis
      
    • CODE:   N02.9
      CODE DESCRIPTION:   
      Recurrent and persistent hematuria with unspecified morphologic changes
      
    • CODE:   N03.0
      CODE DESCRIPTION:   
      Chronic nephritic syndrome with minor glomerular abnormality
      
    • CODE:   N03.1
      CODE DESCRIPTION:   
      Chronic nephritic syndrome with focal and segmental glomerular lesions
      
    • CODE:   N03.2
      CODE DESCRIPTION:   
      Chronic nephritic syndrome with diffuse membranous glomerulonephritis
      
    • CODE:   N03.3
      CODE DESCRIPTION:   
      Chronic nephritic syndrome with diffuse mesangial proliferative glomerulonephritis
      
    • CODE:   N03.4
      CODE DESCRIPTION:   
      Chronic nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis
      
    • CODE:   N03.5
      CODE DESCRIPTION:   
      Chronic nephritic syndrome with diffuse mesangiocapillary glomerulonephritis
      
    • CODE:   N03.6
      CODE DESCRIPTION:   
      Chronic nephritic syndrome with dense deposit disease
      
    • CODE:   N03.7
      CODE DESCRIPTION:   
      Chronic nephritic syndrome with diffuse crescentic glomerulonephritis
      
    • CODE:   N03.8
      CODE DESCRIPTION:   
      Chronic nephritic syndrome with other morphologic changes
      
    • CODE:   N00.3
      CODE DESCRIPTION:   
      Acute nephritic syndrome with diffuse mesangial proliferative glomerulonephritis
      
    • CODE:   N03.9
      CODE DESCRIPTION:   
      Chronic nephritic syndrome with unspecified morphologic changes
      
    • CODE:   N04.0
      CODE DESCRIPTION:   
      Nephrotic syndrome with minor glomerular abnormality
      
    • CODE:   N04.1
      CODE DESCRIPTION:   
      Nephrotic syndrome with focal and segmental glomerular lesions
      
    • CODE:   N04.2
      CODE DESCRIPTION:   
      Nephrotic syndrome with diffuse membranous glomerulonephritis
      
    • CODE:   N04.3
      CODE DESCRIPTION:   
      Nephrotic syndrome with diffuse mesangial proliferative glomerulonephritis
      
    • CODE:   N04.4
      CODE DESCRIPTION:   
      Nephrotic syndrome with diffuse endocapillary proliferative glomerulonephritis
      
    • CODE:   N04.5
      CODE DESCRIPTION:   
      Nephrotic syndrome with diffuse mesangiocapillary glomerulonephritis
      
    • CODE:   N04.6
      CODE DESCRIPTION:   
      Nephrotic syndrome with dense deposit disease
      
    • CODE:   N04.7
      CODE DESCRIPTION:   
      Nephrotic syndrome with diffuse crescentic glomerulonephritis
      
    • CODE:   N04.8
      CODE DESCRIPTION:   
      Nephrotic syndrome with other morphologic changes
      
    • CODE:   N00.4
      CODE DESCRIPTION:   
      Acute nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis
      
    • CODE:   N04.9
      CODE DESCRIPTION:   
      Nephrotic syndrome with unspecified morphologic changes
      
    • CODE:   N05.0
      CODE DESCRIPTION:   
      Unspecified nephritic syndrome with minor glomerular abnormality
      
    • CODE:   N05.1
      CODE DESCRIPTION:   
      Unspecified nephritic syndrome with focal and segmental glomerular lesions
      
    • CODE:   N05.2
      CODE DESCRIPTION:   
      Unspecified nephritic syndrome with diffuse membranous glomerulonephritis
      
    • CODE:   N05.3
      CODE DESCRIPTION:   
      Unspecified nephritic syndrome with diffuse mesangial proliferative glomerulonephritis
      
    • CODE:   N05.4
      CODE DESCRIPTION:   
      Unspecified nephritic syndrome with diffuse endocapillary proliferative 
      glomerulonephritis
      
    • CODE:   N05.5
      CODE DESCRIPTION:   
      Unspecified nephritic syndrome with diffuse mesangiocapillary glomerulonephritis
      
    • CODE:   N05.6
      CODE DESCRIPTION:   
      Unspecified nephritic syndrome with dense deposit disease
      
    • CODE:   N05.7
      CODE DESCRIPTION:   
      Unspecified nephritic syndrome with diffuse crescentic glomerulonephritis
      
    • CODE:   N05.8
      CODE DESCRIPTION:   
      Unspecified nephritic syndrome with other morphologic changes
      
    • CODE:   N00.5
      CODE DESCRIPTION:   
      Acute nephritic syndrome with diffuse mesangiocapillary glomerulonephritis
      
    • CODE:   N05.9
      CODE DESCRIPTION:   
      Unspecified nephritic syndrome with unspecified morphologic changes
      
    • CODE:   N06.0
      CODE DESCRIPTION:   
      Isolated proteinuria with minor glomerular abnormality
      
    • CODE:   N06.1
      CODE DESCRIPTION:   
      Isolated proteinuria with focal and segmental glomerular lesions
      
    • CODE:   N06.2
      CODE DESCRIPTION:   
      Isolated proteinuria with diffuse membranous glomerulonephritis
      
    • CODE:   N06.3
      CODE DESCRIPTION:   
      Isolated proteinuria with diffuse mesangial proliferative glomerulonephritis
      
    • CODE:   N06.4
      CODE DESCRIPTION:   
      Isolated proteinuria with diffuse endocapillary proliferative glomerulonephritis
      
    • CODE:   N06.5
      CODE DESCRIPTION:   
      Isolated proteinuria with diffuse mesangiocapillary glomerulonephritis
      
    • CODE:   N06.6
      CODE DESCRIPTION:   
      Isolated proteinuria with dense deposit disease
      
    • CODE:   N06.7
      CODE DESCRIPTION:   
      Isolated proteinuria with diffuse crescentic glomerulonephritis
      
    • CODE:   N06.8
      CODE DESCRIPTION:   
      Isolated proteinuria with other morphologic lesion
      
    • CODE:   N00.6
      CODE DESCRIPTION:   
      Acute nephritic syndrome with dense deposit disease
      
    • CODE:   N06.9
      CODE DESCRIPTION:   
      Isolated proteinuria with unspecified morphologic lesion
      
    • CODE:   N07.0
      CODE DESCRIPTION:   
      Hereditary nephropathy, not elsewhere classified with minor glomerular 
      abnormality
      
    • CODE:   N07.1
      CODE DESCRIPTION:   
      Hereditary nephropathy, not elsewhere classified with focal and segmental 
      glomerular lesions
      
    • CODE:   N07.2
      CODE DESCRIPTION:   
      Hereditary nephropathy, not elsewhere classified with diffuse membranous 
      glomerulonephritis
      
    • CODE:   N07.3
      CODE DESCRIPTION:   
      Hereditary nephropathy, not elsewhere classified with diffuse mesangial 
      proliferative glomerulonephritis
      
    • CODE:   N07.4
      CODE DESCRIPTION:   
      Hereditary nephropathy, not elsewhere classified with diffuse endocapillary 
      proliferative glomerulonephritis
      
    • CODE:   N07.5
      CODE DESCRIPTION:   
      Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary 
      glomerulonephritis
      
    • CODE:   N07.6
      CODE DESCRIPTION:   
      Hereditary nephropathy, not elsewhere classified with dense deposit disease
      
    • CODE:   N07.7
      CODE DESCRIPTION:   
      Hereditary nephropathy, not elsewhere classified with diffuse crescentic 
      glomerulonephritis
      
    • CODE:   N07.8
      CODE DESCRIPTION:   
      Hereditary nephropathy, not elsewhere classified with other morphologic lesions
      
    • CODE:   N00.7
      CODE DESCRIPTION:   
      Acute nephritic syndrome with diffuse crescentic glomerulonephritis
      
    • CODE:   N07.9
      CODE DESCRIPTION:   
      Hereditary nephropathy, not elsewhere classified with unspecified morphologic 
      lesions
      
    • CODE:   N08
      CODE DESCRIPTION:   
      Glomerular disorders in diseases classified elsewhere
      
    • CODE:   N25.0
      CODE DESCRIPTION:   
      Renal osteodystrophy
      
    • CODE:   N25.1
      CODE DESCRIPTION:   
      Nephrogenic diabetes insipidus
      
    • CODE:   N25.81
      CODE DESCRIPTION:   
      Secondary hyperparathyroidism of renal origin
      
    • CODE:   N25.89
      CODE DESCRIPTION:   
      Other disorders resulting from impaired renal tubular function
      
    • CODE:   N25.9
      CODE DESCRIPTION:   
      Disorder resulting from impaired renal tubular function, unspecified
      
    • CODE:   N00.8
      CODE DESCRIPTION:   
      Acute nephritic syndrome with other morphologic changes
      
MEASURE LIST