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PedAM

Pediatric Disease Annotations & Medicines



   membranoproliferative glomerulonephritis
  

Disease ID 599
Disease membranoproliferative glomerulonephritis
Definition
Chronic glomerulonephritis characterized histologically by proliferation of MESANGIAL CELLS, increase in the MESANGIAL EXTRACELLULAR MATRIX, and a thickening of the glomerular capillary walls. This may appear as a primary disorder or secondary to other diseases including infections and autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Various subtypes are classified by their abnormal ultrastructures and immune deposits. Hypocomplementemia is a characteristic feature of all types of MPGN.
Synonym
chronic glomerulonephritis, lobular
glomerulonephritides, hypocomplementemic
glomerulonephritides, membranoproliferative
glomerulonephritides, mesangiocapillary
glomerulonephritis, hypocomplementemic
glomerulonephritis, hypocomplementemic, chronic
glomerulonephritis, membranoproliferative
glomerulonephritis, membranoproliferative [disease/finding]
glomerulonephritis, mesangiocapillary
hypocomplementemic glomerulonephritides
hypocomplementemic glomerulonephritis
lobular glomerulonephritis
mcgn
mcgn - mesangiocapillary glomerulonephritis
membranoproliferative glomerulonephritides
membranoproliferative glomerulonephritis (mpgn)
membranoproliferative glomerulonephritis nos
mesangiocapillary glomerulonephritides
mesangiocapillary glomerulonephritis
mesangiocapillary glomerulonephritis (disorder)
mesangiocapillary glomerulonephritis, nos
mpgn
mpgn - membranoproliferative glomerulonephritis
DOID
UMLS
C0017662
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:34)
C0010403  |  cryoglobulinemia  |  7
C0027726  |  nephrotic syndrome  |  3
C0019158  |  hepatitis  |  3
C0022658  |  nephropathy  |  2
C0010403  |  cryoglobulinaemia  |  2
C0019196  |  hepatitis c  |  2
C0038463  |  strongyloidiasis  |  2
C0035078  |  renal failure  |  2
C0017658  |  glomerulonephritis  |  2
C1136085  |  monoclonal gammopathy  |  2
C0022658  |  renal disease  |  1
C0022661  |  chronic renal failure  |  1
C0019061  |  hemolytic uremic syndrome  |  1
C0041228  |  african trypanosomiasis  |  1
C0042769  |  virus infection  |  1
C0334634  |  mantle cell lymphoma  |  1
C0020676  |  hypothyroidism  |  1
C0024198  |  lyme disease  |  1
C0022661  |  end-stage renal disease  |  1
C0032463  |  polycythaemia vera  |  1
C0001126  |  renal tubular acidosis  |  1
C0027121  |  myositis  |  1
C0920350  |  autoimmune thyroiditis  |  1
C0041227  |  trypanosomiasis  |  1
C0007102  |  colon cancer  |  1
C1389280  |  basal ganglia calcification  |  1
C1527336  |  sjogren's syndrome  |  1
C0021400  |  influenza  |  1
C0015974  |  periodic fever  |  1
C0011633  |  dermatomyositis  |  1
C0796004  |  kabuki syndrome  |  1
C0019163  |  hepatitis b  |  1
C0032461  |  polycythaemia  |  1
C0021053  |  immune disease  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:5)
PON1  |  5444  |  CTD_human
ALB  |  213  |  CTD_human
C1QA  |  712  |  CTD_human
CFH  |  3075  |  CTD_human
TSLP  |  85480  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:105)
3385  |  ICAM3  |  DISEASES
4210  |  MEFV  |  DISEASES
973  |  CD79A  |  DISEASES
727  |  C5  |  DISEASES
7448  |  VTN  |  DISEASES
4598  |  MVK  |  DISEASES
5657  |  PRTN3  |  DISEASES
1846  |  DUSP4  |  DISEASES
718  |  C3  |  DISEASES
5199  |  CFP  |  DISEASES
968  |  CD68  |  DISEASES
1215  |  CMA1  |  DISEASES
5894  |  RAF1  |  DISEASES
10343  |  PKDREJ  |  DISEASES
6341  |  SCO1  |  DISEASES
4608  |  MYBPH  |  DISEASES
81494  |  CFHR5  |  DISEASES
5959  |  RDH5  |  DISEASES
2799  |  GNS  |  DISEASES
3569  |  IL6  |  DISEASES
3685  |  ITGAV  |  DISEASES
4069  |  LYZ  |  DISEASES
10162  |  LPCAT3  |  DISEASES
9172  |  MYOM2  |  DISEASES
23523  |  CABIN1  |  DISEASES
55717  |  WDR11  |  DISEASES
3383  |  ICAM1  |  DISEASES
6687  |  SPG7  |  DISEASES
57530  |  CGN  |  DISEASES
5972  |  REN  |  DISEASES
3439  |  IFNA1  |  DISEASES
3934  |  LCN2  |  DISEASES
710  |  SERPING1  |  DISEASES
9056  |  SLC7A7  |  DISEASES
715  |  C1R  |  DISEASES
1636  |  ACE  |  DISEASES
6285  |  S100B  |  DISEASES
1234  |  CCR5  |  DISEASES
3046  |  HBE1  |  DISEASES
5937  |  RBMS1  |  DISEASES
213  |  ALB  |  DISEASES
7098  |  TLR3  |  DISEASES
203286  |  ANKS6  |  DISEASES
717  |  C2  |  DISEASES
661  |  POLR3D  |  DISEASES
56945  |  MRPS22  |  DISEASES
4327  |  MMP19  |  DISEASES
4179  |  CD46  |  DISEASES
10294  |  DNAJA2  |  DISEASES
3078  |  CFHR1  |  DISEASES
6014  |  RIT2  |  DISEASES
716  |  C1S  |  DISEASES
29940  |  DSE  |  DISEASES
85480  |  TSLP  |  DISEASES
6575  |  SLC20A2  |  DISEASES
6614  |  SIGLEC1  |  DISEASES
921  |  CD5  |  DISEASES
26762  |  HAVCR1  |  DISEASES
2335  |  FN1  |  DISEASES
5265  |  SERPINA1  |  DISEASES
3683  |  ITGAL  |  DISEASES
23556  |  PIGN  |  DISEASES
2526  |  FUT4  |  DISEASES
10724  |  MGEA5  |  DISEASES
4283  |  CXCL9  |  DISEASES
58  |  ACTA1  |  DISEASES
1378  |  CR1  |  DISEASES
10877  |  CFHR4  |  DISEASES
10878  |  CFHR3  |  DISEASES
3075  |  CFH  |  DISEASES
7827  |  NPHS2  |  DISEASES
284486  |  THEM5  |  DISEASES
4942  |  OAT  |  DISEASES
7272  |  TTK  |  DISEASES
959  |  CD40LG  |  DISEASES
11093  |  ADAMTS13  |  DISEASES
2889  |  RAPGEF1  |  DISEASES
286204  |  CRB2  |  DISEASES
4153  |  MBL2  |  DISEASES
7056  |  THBD  |  DISEASES
8718  |  TNFRSF25  |  DISEASES
83715  |  ESPN  |  DISEASES
4868  |  NPHS1  |  DISEASES
3440  |  IFNA2  |  DISEASES
3456  |  IFNB1  |  DISEASES
51199  |  NIN  |  DISEASES
3426  |  CFI  |  DISEASES
3029  |  HAGH  |  DISEASES
340990  |  OTOG  |  DISEASES
25983  |  NGDN  |  DISEASES
255743  |  NPNT  |  DISEASES
720  |  C4A  |  DISEASES
960  |  CD44  |  DISEASES
3106  |  HLA-B  |  DISEASES
2821  |  GPI  |  DISEASES
7148  |  TNXB  |  DISEASES
5270  |  SERPINE2  |  DISEASES
721  |  C4B  |  DISEASES
629  |  CFB  |  DISEASES
4925  |  NUCB2  |  DISEASES
8972  |  MGAM  |  DISEASES
51499  |  TRIAP1  |  DISEASES
2585  |  GALK2  |  DISEASES
4782  |  NFIC  |  DISEASES
677807  |  SNORA22  |  DISEASES
Locus(Waiting for update.)
Disease ID 599
Disease membranoproliferative glomerulonephritis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:21)
HP:0100778  |  Cryoglobulinemia  |  7
HP:0000100  |  Nephrosis  |  3
HP:0012115  |  Liver inflammation  |  3
HP:0003774  |  End-stage renal failure  |  2
HP:0000112  |  Nephropathy  |  2
HP:0000099  |  Glomerular nephritis  |  2
HP:0000083  |  Renal insufficiency  |  2
HP:0002135  |  Basal ganglia calcification  |  1
HP:0012597  |  Heavy proteinuria  |  1
HP:0100699  |  Scarring  |  1
HP:0002049  |  Proximal renal tubular acidosis  |  1
HP:0001941  |  acidemia  |  1
HP:0011510  |  Drusen  |  1
HP:0003003  |  Colon cancer  |  1
HP:0002960  |  Autoimmune condition  |  1
HP:0001947  |  Renal tubular acidosis  |  1
HP:0100614  |  Muscle inflammation  |  1
HP:0100820  |  Glomerulopathy  |  1
HP:0001945  |  Fever  |  1
HP:0005575  |  Hemolytic-uremic syndrome  |  1
HP:0000821  |  Underactive thyroid  |  1
Disease ID 599
Disease membranoproliferative glomerulonephritis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:16)
C1963154  |  renal failure
C1963084  |  colitis
C1962972  |  proteinuria
C1962966  |  retinopathy
C1623038  |  cirrhosis
C0268731  |  glomerular diseases
C0264383  |  organizing pneumonia
C0085679  |  hyperchloremia
C0085404  |  crow-fukase syndrome
C0039263  |  takayasu's arteritis
C0036330  |  schistosoma mansoni infection
C0027726  |  nephrotic syndrome
C0022661  |  end-stage renal disease
C0022661  |  chronic renal failure
C0022660  |  acute renal failure
C0010403  |  cryoglobulinemia
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:5)
C0010403  |  cryoglobulinemia  |  7
C0027726  |  nephrotic syndrome  |  3
C0035078  |  renal failure  |  2
C0022661  |  end-stage renal disease  |  1
C0022661  |  chronic renal failure  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:7)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0017662creatineD00340157-00-1glomerulonephritis, membranoproliferativeMESH:D015432marker/mechanism14725210
C0017662phenytoinD01067257-41-0glomerulonephritis, membranoproliferativeMESH:D015432marker/mechanism7099337
C0017662sirolimusD02012353123-88-9glomerulonephritis, membranoproliferativeMESH:D015432marker/mechanism15112032
C0017662spironolactoneD0131481952/1/7glomerulonephritis, membranoproliferativeMESH:D015432therapeutic16928621
C0017662tacrolimusD016559109581-93-3glomerulonephritis, membranoproliferativeMESH:D015432therapeutic19406543
C0017662tretinoinD014212302-79-4glomerulonephritis, membranoproliferativeMESH:D015432marker/mechanism17686814
C0017662valsartanD000068756-glomerulonephritis, membranoproliferativeMESH:D015432therapeutic16928621
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)