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Immunoglobulin-mediated membranoproliferative glomerulonephritis
1 OMIM reference -
2 associated genes
No signs/symptoms info
COMMON GENES: 1
Atypical hemolytic uremic syndrome with DGKE deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Immunoglobulin-mediated membranoproliferative glomerulonephritis
Atypical hemolytic uremic syndrome with DGKE deficiency

CFH
(UniProt - OMIM)
 DGKE
(UniProt - OMIM)
DGKE
(UniProt - OMIM)

COMMON
GENES 		DGKE


Citations in the biomedical literature:


Immunoglobulin-mediated membranoproliferative glomerulonephritis
CFH DGKE
Atypical hemolytic uremic syndrome with DGKE deficiency



Immunoglobulin-mediated membranoproliferative glomerulonephritis
Atypical hemolytic uremic syndrome with DGKE deficiency

Synonym(s):
- Ig-mediated MPGN
- Ig-mediated membranoproliferative glomerulonephritis
- Immunoglobulin-mediated MPGN
Synonym(s):
- Atypical HUS with DGKE deficiency
- D-HUS with DGKE deficiency
- Hemolytic-uremic syndrome without diarrhea with DGKE deficiency
- aHUS with DGKE deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.