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Immunodeficiency with factor H anomaly
1 OMIM reference -
1 associated gene
17 connected diseases
No signs/symptoms info
Disease Type of connection
Dense deposit disease
Atypical hemolytic uremic syndrome with H factor anomaly
Familial drusen
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
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare immune 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:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
CFH P08603134370
No signs/symptoms info available.