Cytoscape Web
Click node...

Dense deposit disease
1 OMIM reference -
2 associated genes
20 connected diseases
No signs/symptoms info
Disease Type of connection
Atypical hemolytic uremic syndrome with H factor anomaly
Atypical hemolytic uremic syndrome with anti-factor H antibodies
C3 glomerulonephritis
Familial drusen
Immunodeficiency with factor H anomaly
Immunoglobulin-mediated membranoproliferative glomerulonephritis
Atypical hemolytic uremic syndrome with C3 anomaly
Complement component 3 deficiency
Congenital analbuminemia
Acute promyelocytic leukemia
Aneurysm - osteoarthritis syndrome
Familial thoracic aortic aneurysm and aortic dissection
Hypocalcemic vitamin D-resistant rickets
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Apolipoprotein A-I deficiency
Atypical hemolytic uremic syndrome with I factor anomaly
Familial renal amyloidosis due to Apolipoprotein AI variant
Immunodeficiency with factor I anomaly
Primary systemic amyloidosis
Autosomal recessive hypophosphatemic rickets
Synonym(s):
- Membranoproliferative glomerulonephritis type 2
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
1 MeSH reference: D015432
Gene symbol UniProt reference OMIM reference
CFH P08603134370
CFHR1 Q03591134371
No signs/symptoms info available.