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Atypical hemolytic uremic syndrome with H factor anomaly
2 OMIM references -
1 associated gene
17 connected diseases
No signs/symptoms info
Disease Type of connection
Dense deposit disease
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
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):
- Atypical HUS with H factor anomaly
- D-HUS with H factor anomaly
- Hemolytic-uremic syndrome without diarrhea with H factor anomaly
- aHUS with H factor anomaly
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
CFH P08603134370
No signs/symptoms info available.