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Immunodeficiency due to a late component of complements deficiency
6 OMIM references -
7 associated genes
12 connected diseases
No signs/symptoms info
Disease Type of connection
Primary CD59 deficiency
Fibronectin glomerulopathy
Atypical hemolytic uremic syndrome with C3 anomaly
Complement component 3 deficiency
Hypoplasminogenemia
Ligneous conjunctivitis
Chronic myeloid leukemia
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Immunodeficiency due to an early component of complement deficiency
Cerebral sinovenous thrombosis
Congenital factor II deficiency
Synonym(s):
- Deficiency of complement of terminal pathway
- Immunodeficiency due to a C5 to C9 component complement deficiency
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:
6 OMIM references -
No MeSH references
No signs/symptoms info available.