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Pediatric Disease Annotations & Medicines



   membranous nephropathy
  

Disease ID 247
Disease membranous nephropathy
Definition
A type of glomerulonephritis that is characterized by the accumulation of immune deposits (COMPLEMENT MEMBRANE ATTACK COMPLEX) on the outer aspect of the GLOMERULAR BASEMENT MEMBRANE. It progresses from subepithelial dense deposits, to basement membrane reaction and eventual thickening of the basement membrane.
Synonym
chronic nephritic syndrome, diffuse membranous glomerulonephritis
chronic nephritic syndrome, diffuse membranous glomerulonephritis (disorder)
extramembranous glomerulopathy
glomerulonephritides, membranous
glomerulonephritis membranous
glomerulonephritis, membranous
glomerulonephritis, membranous [disease/finding]
glomerulonephropathy, membranous
glomerulopathy, extramembranous
glomerulopathy, membranous
membranous glomerulonephritides
membranous glomerulonephritis
membranous glomerulonephritis (disorder)
membranous glomerulonephritis nos
membranous glomerulonephropathy
membranous glomerulopathy
membranous nephropathy nos
mgn
mgn - membranous glomerulonephritis
nephropathy, membranous
DOID
UMLS
C0017665
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:52)
C0027726  |  nephrotic syndrome  |  35
C0033687  |  proteinuria  |  9
C0017658  |  glomerulonephritis  |  7
C0027697  |  nephritis  |  7
C0027707  |  interstitial nephritis  |  4
C0022658  |  kidney disease  |  3
C0008312  |  primary biliary cirrhosis  |  3
C0022658  |  renal disease  |  3
C0019163  |  hepatitis b  |  3
C0041349  |  tubulointerstitial nephritis  |  3
C0019158  |  hepatitis  |  3
C0008312  |  biliary cirrhosis  |  3
C0042384  |  vasculitis  |  2
C0022661  |  end-stage renal disease  |  2
C0024141  |  systemic lupus erythematosus  |  2
C0033838  |  kimura's disease  |  2
C0023890  |  cirrhosis  |  2
C0022679  |  cystic kidney  |  2
C0026709  |  mucopolysaccharidosis type vi  |  1
C0040156  |  thyrotoxicosis  |  1
C0152025  |  polyneuropathy  |  1
C0398623  |  hypercoagulable state  |  1
C1509147  |  histiocytoma  |  1
C0270922  |  demyelinating polyneuropathy  |  1
C0206644  |  fibrous histiocytoma  |  1
C0524988  |  schnitzler syndrome  |  1
C0017662  |  membranoproliferative glomerulonephritis  |  1
C0041234  |  chagas disease  |  1
C0009402  |  colorectal cancer  |  1
C0023418  |  leukemia  |  1
C0032027  |  pityriasis rubra pilaris  |  1
C0235618  |  proliferative glomerulonephritis  |  1
C0018378  |  guillain-barre syndrome  |  1
C0008728  |  churg-strauss syndrome  |  1
C0677607  |  hashimoto's thyroiditis  |  1
C0041296  |  tuberculosis  |  1
C0023448  |  lymphocytic leukemia  |  1
C0403529  |  goodpasture's disease  |  1
C0023895  |  liver disease  |  1
C0178664  |  glomerulosclerosis  |  1
C0017661  |  iga nephropathy  |  1
C0023434  |  chronic lymphocytic leukemia  |  1
C0011881  |  diabetic kidney disease  |  1
C0026703  |  mucopolysaccharidosis  |  1
C0393819  |  chronic inflammatory demyelinating polyneuropathy  |  1
C0035078  |  renal failure  |  1
C1565489  |  renal insufficiency  |  1
C0302592  |  cervical ca  |  1
C0017668  |  focal segmental glomerulosclerosis  |  1
C0949691  |  spondyloarthropathy  |  1
C0007113  |  rectal cancer  |  1
C0007847  |  cervical cancer  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:5)
HLA-DRB1  |  3123  |  CTD_human
HLA-DQA1  |  3117  |  CTD_human
APOA1  |  335  |  CTD_human
ALB  |  213  |  CTD_human
GAA  |  2548  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:3)
1286  |  COL4A4  |  infer
3117  |  HLA-DQA1  |  infer
22925  |  PLA2R1  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:181)
3385  |  ICAM3  |  DISEASES
7038  |  TG  |  DISEASES
2217  |  FCGRT  |  DISEASES
7040  |  TGFB1  |  DISEASES
973  |  CD79A  |  DISEASES
4353  |  MPO  |  DISEASES
6347  |  CCL2  |  DISEASES
7448  |  VTN  |  DISEASES
3558  |  IL2  |  DISEASES
9450  |  LY86  |  DISEASES
3565  |  IL4  |  DISEASES
2908  |  NR3C1  |  DISEASES
5657  |  PRTN3  |  DISEASES
2023  |  ENO1  |  DISEASES
29094  |  LGALSL  |  DISEASES
718  |  C3  |  DISEASES
10047  |  CST8  |  DISEASES
391013  |  PLA2G2C  |  DISEASES
968  |  CD68  |  DISEASES
3998  |  LMAN1  |  DISEASES
81  |  ACTN4  |  DISEASES
10343  |  PKDREJ  |  DISEASES
3975  |  LHX1  |  DISEASES
182  |  JAG1  |  DISEASES
4608  |  MYBPH  |  DISEASES
81494  |  CFHR5  |  DISEASES
2799  |  GNS  |  DISEASES
3915  |  LAMC1  |  DISEASES
3569  |  IL6  |  DISEASES
27283  |  TINAG  |  DISEASES
3685  |  ITGAV  |  DISEASES
4069  |  LYZ  |  DISEASES
9097  |  USP14  |  DISEASES
114294  |  LACTB  |  DISEASES
3959  |  LGALS3BP  |  DISEASES
23523  |  CABIN1  |  DISEASES
9466  |  IL27RA  |  DISEASES
4036  |  LRP2  |  DISEASES
4811  |  NID1  |  DISEASES
8916  |  HERC3  |  DISEASES
5443  |  POMC  |  DISEASES
3383  |  ICAM1  |  DISEASES
2028  |  ENPEP  |  DISEASES
8395  |  PIP5K1B  |  DISEASES
92912  |  UBE2Q2  |  DISEASES
6687  |  SPG7  |  DISEASES
8547  |  FCN3  |  DISEASES
57530  |  CGN  |  DISEASES
29956  |  CERS2  |  DISEASES
5972  |  REN  |  DISEASES
9027  |  NAT8  |  DISEASES
185  |  AGTR1  |  DISEASES
80854  |  SETD7  |  DISEASES
3439  |  IFNA1  |  DISEASES
3934  |  LCN2  |  DISEASES
5800  |  PTPRO  |  DISEASES
7082  |  TJP1  |  DISEASES
22925  |  PLA2R1  |  DISEASES
7345  |  UCHL1  |  DISEASES
231  |  AKR1B1  |  DISEASES
1636  |  ACE  |  DISEASES
643  |  CXCR5  |  DISEASES
3046  |  HBE1  |  DISEASES
6352  |  CCL5  |  DISEASES
58191  |  CXCL16  |  DISEASES
213  |  ALB  |  DISEASES
57619  |  SHROOM3  |  DISEASES
5267  |  SERPINA4  |  DISEASES
3429  |  IFI27  |  DISEASES
7184  |  HSP90B1  |  DISEASES
915  |  CD3D  |  DISEASES
51129  |  ANGPTL4  |  DISEASES
661  |  POLR3D  |  DISEASES
4330  |  MN1  |  DISEASES
1602  |  DACH1  |  DISEASES
7275  |  TUB  |  DISEASES
7369  |  UMOD  |  DISEASES
157570  |  ESCO2  |  DISEASES
54205  |  CYCS  |  DISEASES
5340  |  PLG  |  DISEASES
118430  |  MUCL1  |  DISEASES
5319  |  PLA2G1B  |  DISEASES
64236  |  PDLIM2  |  DISEASES
1191  |  CLU  |  DISEASES
8542  |  APOL1  |  DISEASES
9377  |  COX5A  |  DISEASES
28959  |  TMEM176B  |  DISEASES
7173  |  TPO  |  DISEASES
147179  |  WIPF2  |  DISEASES
3321  |  IGSF3  |  DISEASES
64089  |  SNX16  |  DISEASES
2  |  A2M  |  DISEASES
3309  |  HSPA5  |  DISEASES
51330  |  TNFRSF12A  |  DISEASES
1668  |  DEFA3  |  DISEASES
7490  |  WT1  |  DISEASES
5271  |  SERPINB8  |  DISEASES
8214  |  DGCR6  |  DISEASES
6401  |  SELE  |  DISEASES
80128  |  TRIM46  |  DISEASES
8710  |  SERPINB7  |  DISEASES
64412  |  GZF1  |  DISEASES
3117  |  HLA-DQA1  |  DISEASES
966  |  CD59  |  DISEASES
7335  |  UBE2V1  |  DISEASES
26578  |  OSTF1  |  DISEASES
7225  |  TRPC6  |  DISEASES
26762  |  HAVCR1  |  DISEASES
55561  |  CDC42BPG  |  DISEASES
5265  |  SERPINA1  |  DISEASES
3240  |  HP  |  DISEASES
23556  |  PIGN  |  DISEASES
55243  |  KIRREL  |  DISEASES
23607  |  CD2AP  |  DISEASES
4311  |  MME  |  DISEASES
9181  |  ARHGEF2  |  DISEASES
10724  |  MGEA5  |  DISEASES
5891  |  MOK  |  DISEASES
88  |  ACTN2  |  DISEASES
1378  |  CR1  |  DISEASES
5321  |  PLA2G4A  |  DISEASES
7827  |  NPHS2  |  DISEASES
6675  |  UAP1  |  DISEASES
1490  |  CTGF  |  DISEASES
922  |  CD5L  |  DISEASES
4942  |  OAT  |  DISEASES
9748  |  SLK  |  DISEASES
959  |  CD40LG  |  DISEASES
8569  |  MKNK1  |  DISEASES
286204  |  CRB2  |  DISEASES
27293  |  SMPDL3B  |  DISEASES
4153  |  MBL2  |  DISEASES
3339  |  HSPG2  |  DISEASES
3118  |  HLA-DQA2  |  DISEASES
3127  |  HLA-DRB5  |  DISEASES
5320  |  PLA2G2A  |  DISEASES
23509  |  POFUT1  |  DISEASES
50943  |  FOXP3  |  DISEASES
7133  |  TNFRSF1B  |  DISEASES
3105  |  HLA-A  |  DISEASES
8718  |  TNFRSF25  |  DISEASES
5420  |  PODXL  |  DISEASES
4868  |  NPHS1  |  DISEASES
375790  |  AGRN  |  DISEASES
3440  |  IFNA2  |  DISEASES
5272  |  SERPINB9  |  DISEASES
348801  |  LNP1  |  DISEASES
22908  |  SACM1L  |  DISEASES
284217  |  LAMA1  |  DISEASES
28227  |  PPP2R3B  |  DISEASES
51429  |  SNX9  |  DISEASES
162239  |  ZFP1  |  DISEASES
11346  |  SYNPO  |  DISEASES
87  |  ACTN1  |  DISEASES
6696  |  SPP1  |  DISEASES
152330  |  CNTN4  |  DISEASES
8091  |  HMGA2  |  DISEASES
2909  |  ARHGAP35  |  DISEASES
7018  |  TF  |  DISEASES
154810  |  AMOTL1  |  DISEASES
255743  |  NPNT  |  DISEASES
8399  |  PLA2G10  |  DISEASES
25801  |  GCA  |  DISEASES
720  |  C4A  |  DISEASES
960  |  CD44  |  DISEASES
7124  |  TNF  |  DISEASES
387  |  RHOA  |  DISEASES
3609  |  ILF3  |  DISEASES
221981  |  THSD7A  |  DISEASES
3115  |  HLA-DPB1  |  DISEASES
721  |  C4B  |  DISEASES
629  |  CFB  |  DISEASES
7029  |  TFDP2  |  DISEASES
51428  |  DDX41  |  DISEASES
84000  |  TMPRSS13  |  DISEASES
930  |  CD19  |  DISEASES
80790  |  CMIP  |  DISEASES
8742  |  TNFSF12  |  DISEASES
4157  |  MC1R  |  DISEASES
567  |  B2M  |  DISEASES
3949  |  LDLR  |  DISEASES
Locus(Waiting for update.)
Disease ID 247
Disease membranous nephropathy
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:35)
HP:0000100  |  Nephrosis  |  35
HP:0000093  |  Proteinuria  |  9
HP:0000123  |  Nephritis  |  7
HP:0000099  |  Glomerular nephritis  |  6
HP:0001970  |  Interstitial nephritis  |  4
HP:0001907  |  Thromboembolic disease  |  3
HP:0002613  |  Biliary cirrhosis  |  3
HP:0012115  |  Liver inflammation  |  3
HP:0002633  |  Vasculitis  |  2
HP:0003774  |  End-stage renal failure  |  2
HP:0002960  |  Autoimmune condition  |  2
HP:0000083  |  Renal insufficiency  |  2
HP:0002725  |  Systemic lupus erythematosus  |  2
HP:0000113  |  Polycystic kidney dysplasia  |  2
HP:0001394  |  Hepatic cirrhosis  |  2
HP:0200123  |  Chronic liver inflammation  |  2
HP:0000127  |  Salt wasting  |  1
HP:0001271  |  Polyneuropathy  |  1
HP:0012588  |  Steroid-resistant nephrotic syndrome  |  1
HP:0002664  |  Neoplasia  |  1
HP:0012593  |  Nephrotic range proteinuria  |  1
HP:0001289  |  Confusion  |  1
HP:0100615  |  Neoplasm of the ovary  |  1
HP:0001919  |  Acute renal failure  |  1
HP:0000096  |  Glomerulosclerosis  |  1
HP:0004319  |  Mineralocorticoid insufficiency  |  1
HP:0000097  |  focal glomerulosclerosis  |  1
HP:0000872  |  Hashimoto's thyroiditis  |  1
HP:0005550  |  Chronic lymphatic leukemia  |  1
HP:0012574  |  Mesangial hypercellularity  |  1
HP:0001909  |  Leukemia  |  1
HP:0012315  |  Histiocytoma  |  1
HP:0000793  |  Membranoproliferative glomerulonephritis  |  1
HP:0012597  |  Heavy proteinuria  |  1
HP:0001941  |  acidemia  |  1
Disease ID 247
Disease membranous nephropathy
Manually Symptom
UMLS  | Name(Total Manually Symptoms:35)
C2697391  |  rheumatoid arthritis
C2697310  |  sarcoidosis
C2677535  |  ane syndrome
C1963154  |  renal failure
C1962974  |  chylothorax
C1962972  |  proteinuria
C1561644  |  chronic kidney disease (ckd)
C1417247  |  glomerulosclerosis
C1318533  |  secondary polycythemia
C0949691  |  spondyloarthropathy
C0850666  |  helicobacter pylori infection
C0566602  |  primary sclerosing cholangitis
C0521607  |  peritoneal fibrosis
C0403416  |  crescentic glomerulonephritis
C0268750  |  necrotizing glomerulonephritis
C0265050  |  vena cava thrombosis
C0238457  |  renal vein thrombosis
C0221013  |  systemic mastocytosis
C0206669  |  liver cell adenoma
C0162678  |  neurofibromatosis
C0162557  |  acute hepatic failure
C0149678  |  epstein-barr virus infection
C0041327  |  pulmonary tuberculosis
C0041296  |  tuberculosis
C0040053  |  thrombosis
C0032461  |  polycythaemia
C0030805  |  bullous pemphigoid
C0027831  |  recklinghausen's neurofibromatosis
C0027726  |  nephrotic syndrome
C0027697  |  nephritis
C0022661  |  end-stage renal disease
C0022661  |  chronic renal failure
C0017531  |  angiolymphoid hyperplasia
C0015624  |  fanconi's syndrome
C0011633  |  dermatomyositis
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:9)
C0027726  |  nephrotic syndrome  |  35
C0033687  |  proteinuria  |  9
C0027697  |  nephritis  |  7
C0022661  |  end-stage renal disease  |  2
C0041296  |  tuberculosis  |  1
C0949691  |  spondyloarthropathy  |  1
C0178664  |  glomerulosclerosis  |  1
C0268750  |  necrotizing glomerulonephritis  |  1
C0035078  |  renal failure  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:3)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs397507444215009824524MTHFRumls:C0017665BeFreeCerebral sinovenous thrombosis associated with factor V Leiden and methylenetetrahydrofolate reductase A1298C mutation in adult membranous glomerulonephritis.0.0005428842011MTHFR111794407TG
rs397507444215009822153F5umls:C0017665BeFreeCerebral sinovenous thrombosis associated with factor V Leiden and methylenetetrahydrofolate reductase A1298C mutation in adult membranous glomerulonephritis.0.0005428842011MTHFR111794407TG
rs46643082132354122925PLA2R1umls:C0017665GAD[An HLA-DQA1 allele on chromosome 6p21 is most closely associated with idiopathic membranous nephropathy in persons of white ancestry. This allele may facilitate an autoimmune response against targets such as variants of PLA2R1. Our findings suggest a basi]0.0069055992011PLA2R1;LOC1053737172160060986AG
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:2)
CHR POS SNPID REF ALT ORI_SNPID PMID P_VALUE P_VALUE_TEXT OR/BETA CI95_TEXT GWAS_INITIAL_SAMPLE_SIZE SUB_POPULATION SUPER_POPULATION GWAS_TRAIT HPO_ID HPO_TERM DO_ID DO_TERM MESH_ID MESH_TERM EFO_ID EFO_TERM DOLITE_TERM RISK_ALLELE PUBLICATION_TYPE AA GENE_SYMBOL TYPE REFGENE
2160917497rs4664308AGrs4664308213235419.00E-29NA2.28[1.96-2.64]556 European ancestry cases; 2,338 European ancestry controlsEuropean(2894)ALL(2894)EUR(2894)ALL(2894)Nephropathy (idiopathic membranous)HPOID:0000112NephropathyDOID:10976membranous glomerulonephritisD015433Glomerulonephritis, MembranousEFOID:0004254membranous glomerulonephritisGlomerulonephritisNAResearch Support, Non-U.S. Gov'tAPLA2R1
632605884rs2187668CTrs2187668213235418.00E-93NA4.32[3.73-5.01]556 European ancestry cases; 2,338 European ancestry controlsEuropean(2894)ALL(2894)EUR(2894)ALL(2894)Nephropathy (idiopathic membranous)HPOID:0000112NephropathyDOID:10976membranous glomerulonephritisD015433Glomerulonephritis, MembranousEFOID:0004254membranous glomerulonephritisGlomerulonephritisNAResearch Support, Non-U.S. Gov'tGHLA-DQA1
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:13)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0017665chlorambucilD002699305-03-3glomerulonephritis, membranousMESH:D015433therapeutic17211287
C0017665cyclophosphamideD00352050-18-0glomerulonephritis, membranousMESH:D015433therapeutic16234291
C0017665diclofenacD00400815307-86-5glomerulonephritis, membranousMESH:D015433marker/mechanism7290298
C0017665fenoprofenD00527931879-05-7glomerulonephritis, membranousMESH:D015433marker/mechanism3146734
C0017665fluconazoleD01572586386-73-4glomerulonephritis, membranousMESH:D015433marker/mechanism17261435
C0017665gemcitabineC056507103882-84-4glomerulonephritis, membranousMESH:D015433marker/mechanism10528031
C0017665nabumetoneC03560542924-53-8glomerulonephritis, membranousMESH:D015433marker/mechanism8691554
C0017665propylthiouracilD01144151-52-5glomerulonephritis, membranousMESH:D015433marker/mechanism17472842
C0017665sirolimusD02012353123-88-9glomerulonephritis, membranousMESH:D015433marker/mechanism15112032
C0017665tacrolimusD016559109581-93-3glomerulonephritis, membranousMESH:D015433therapeutic9794552
C0017665tioproninD0086251953/2/2glomerulonephritis, membranousMESH:D015433marker/mechanism2250412
C0017665tolmetinD01404626171-23-3glomerulonephritis, membranousMESH:D015433marker/mechanism8691554
C0017665vinorelbineC03085271486-22-1glomerulonephritis, membranousMESH:D015433marker/mechanism10528031
FDA approved drug and dosage information(Total Drugs:0)
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FDA labeling changes(Total Drugs:0)
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