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Immunoglobulin-mediated membranoproliferative glomerulonephritis
1 OMIM reference -
2 associated genes
21 connected diseases
No signs/symptoms info
Disease Type of connection
Dense deposit disease
Atypical hemolytic uremic syndrome with DGKE deficiency
Atypical hemolytic uremic syndrome with H factor anomaly
Familial drusen
Immunodeficiency with factor H anomaly
Atypical hemolytic uremic syndrome with C3 anomaly
Complement component 3 deficiency
Leigh syndrome with cardiomyopathy
Pyruvate dehydrogenase E1-alpha deficiency
Congenital analbuminemia
Acute promyelocytic leukemia
Aneurysm - osteoarthritis syndrome
Familial thoracic aortic aneurysm and aortic dissection
Hypocalcemic vitamin D-resistant rickets
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Atypical hemolytic uremic syndrome with I factor anomaly
Atypical hemolytic uremic syndrome with anti-factor H antibodies
C3 glomerulonephritis
Immunodeficiency with factor I anomaly
Autosomal recessive hypophosphatemic rickets
Synonym(s):
- Ig-mediated MPGN
- Ig-mediated membranoproliferative glomerulonephritis
- Immunoglobulin-mediated MPGN
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
CFH P08603134370
DGKE P52429601440
No signs/symptoms info available.