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Atypical hemolytic uremic syndrome with MCP/CD46 anomaly
1 OMIM reference -
1 associated gene
13 connected diseases
No signs/symptoms info
Disease Type of connection
Alagille syndrome due to 20p12 microdeletion
Alagille syndrome due to a JAG1 point mutation
Tetralogy of Fallot
Atypical hemolytic uremic syndrome with C3 anomaly
Complement component 3 deficiency
Common variable immunodeficiency
Fetal and neonatal alloimmune thrombocytopenia
Nephrotic syndrome-deafness-pretibial epidermolysis bullosa syndrome
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Larsen syndrome
Boomerang dysplasia
Spondylocarpotarsal synostosis
- Atypical HUS with MCP/CD46 anomaly
- D-HUS with MCP/CD46 anomaly
- Hemolytic-uremic syndrome without diarrhea with MCP/CD46 anomaly
- aHUS with MCP/CD46 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:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
CD46 P15529120920
No signs/symptoms info available.