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Ontology Browser

type I complement component 8 deficiency (DOID:0060301)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
arthus reaction  
atypical hemolytic-uremic syndrome  
C1 inhibitor deficiency +   
complement component 2 deficiency  
complement component 3 deficiency  
Complement Component 4, Partial Deficiency Of  
complement component 4A deficiency  
complement component 4B deficiency  
complement component 5 deficiency  
complement component 6 deficiency  
complement component 7 deficiency  
complement component 9 deficiency  
Complement Component C1r/C1s Deficiency +   
Complement Factor B Deficiency  
Complement Factor D Deficiency  
complement factor I deficiency  
Henoch-Schoenlein purpura +   
hypersensitivity vasculitis +   
Serum Sickness  
type I complement component 8 deficiency  
A complement deficiency that is characterized by deficiency of the alpha subunit of complement protein 8, which causes increased susceptibility to recurrent bacterial infections, especially to Neisseria meningitidis, and has_material_basis_in autosomal recessive inheritance of mutation in the C8A gene, which produces the alpha subunit of complement component 8 important in forming membrane attack complexes. (DO)
type II complement component 8 deficiency  
X-linked properdin deficiency  

Exact Synonyms: C8 ALPHA-GAMMA DEFICIENCY ;   C8 deficiency type I ;   C8AG DEFICIENCY ;   C8D1
Related Synonyms: complement component 8, alpha subunit, A/B polymorphism
Primary IDs: OMIM:613790
Definition Sources: "DO" "DO"

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