Decreased serum complement C3

Symptom Information:

Symptom ID: HPO:0005421
Synonyms:
Decreased serum C3 [HPO:0005421]
Decreased serum C3 [OMIM:Decreased serum C3]
Decreased serum C3 (atypical HUS) [OMIM:Decreased serum C3 (atypical HUS)]
Decreased serum complement C3 (120700) [OMIM:Decreased serum complement C3 (120700)]
Quality:
Cross references:
OMIM: "Decreased serum C3" [OMIM:Decreased serum C3]
OMIM: "Decreased serum C3 (atypical HUS)" [OMIM:Decreased serum C3 (atypical HUS)]
OMIM: "Decreased serum complement C3 (120700)" [OMIM:Decreased serum complement C3 (120700)]
Is a (Direct Parents):
HPO         Complement deficiency
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Abnormality of humoral immunity(HPO:0005368)
                Abnormality of complement system(HPO:0005339)
                   Complement deficiency(HPO:0004431)
                      Decreased serum complement C3(HPO:0005421)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Atypical hemolytic uremic syndrome (Orphanet:2134)
Atypical hemolytic uremic syndrome with H factor anomaly (Orphanet:93579)
Atypical hemolytic uremic syndrome with anti-factor H antibodies (Orphanet:93581)
Complement component 3 deficiency (Orphanet:280133)
Immunodeficiency with factor I anomaly (Orphanet:200418)
LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3,WITH OR WITHOUT GLOMERULONEPHRITIS (OMIM:613913)
Partial acquired lipodystrophy (Orphanet:79087)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Typical hemolytic uremic syndrome (Orphanet:90038)