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PedAM

Pediatric Disease Annotations & Medicines



   dense deposit disease
  

Disease ID 399
Disease dense deposit disease
Definition
A type of membranoproliferative glomerulonephritis characterized by electron dense deposits at the glomerular basement membrane. [Eurenomics:ewuehl, pmid:20301598]
Synonym
ddd mpgnii
dense deposit disease (disorder)
mcgn type ii - mesangiocapillary glomerulonephritis type ii
mcgndd - mesangiocapillary glomerulonephritis, dense deposit
membranoproliferative glomerulonephritis type 2
membranoproliferative glomerulonephritis type ii
membranoproliferative glomerulonephritis, type ii
mesangiocapillary glomerulonephritis type 2
mesangiocapillary glomerulonephritis type ii
mesangiocapillary glomerulonephritis, type ii
mesangiocapillary glomerulonephritis, type ii (disorder)
mpgnii
type ii mpgn
Orphanet
UMLS
C0268743
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:5)
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:2)
CFH  |  3075  |  ORPHANET
CFHR1  |  3078  |  ORPHANET
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus
Symbol | Locus(Total Locus:2)
CFH  |  1q31.3
CFHR1  |  1q31.3
Disease ID 399
Disease dense deposit disease
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:4)
HP:0001919  |  Acute renal failure  |  1
HP:0100820  |  Glomerulopathy  |  1
HP:0000100  |  Nephrosis  |  1
HP:0000083  |  Renal insufficiency  |  1
Disease ID 399
Disease dense deposit disease
Manually Symptom
UMLS  | Name(Total Manually Symptoms:3)
C1963154  |  renal failure
C1373218  |  immunosuppression
C0022660  |  acute renal failure
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:2)
C0022660  |  acute renal failure  |  1
C0035078  |  renal failure  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:4)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1061170224566013075CFHumls:C0268743BeFreeThe complement factor H Y402H variant was significantly increased in dense deposit disease.0.1262431632012CFH1196690107CT
rs386614680212704653075CFHumls:C0268743BeFreeHere, we investigate the consequences of aHUS-linked mutations (R53H and R78G) within the FH N-terminal complement control protein module that also carries the I62V variation linked to dense-deposit disease and age-related macular degeneration.0.1262431632011NANANANANA
rs386614680182527123075CFHumls:C0268743BeFreeSubstitution of buried Val-62 with Ile (a factor H single nucleotide polymorphism potentially protective for age-related macular degeneration and dense deposit disease) causes rearrangements within the module 1 core and increases thermal stability but does not disturb the interface with module 2.0.1262431632008NANANANANA
rs800292212704653075CFHumls:C0268743BeFreeHere, we investigate the consequences of aHUS-linked mutations (R53H and R78G) within the FH N-terminal complement control protein module that also carries the I62V variation linked to dense-deposit disease and age-related macular degeneration.0.1262431632011CFH1196673103GA
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0001919Acute kidney injuryMP:0002135abnormal kidney morphology;HP:0000083Renal insufficiency
Mapped by homologous gene(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0001919Acute kidney injuryMP:0005402abnormal action potential;HP:0000083Renal insufficiency
Chemical(Total Drugs:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)