Anuria
phenotype
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
18
0.100
None
0
Decreased serum complement C3
phenotype
Finding
12
0.100
None
0
Seizures
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
2152
553
0.100
None
0
Thrombocytopenia
phenotype
Hemic and Lymphatic Diseases
Disease or Syndrome
592
110
0.100
None
0
Blood urea increased
phenotype
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Finding
12
0.100
None
0
Reticulocytosis
phenotype
Pathological Conditions, Signs and Symptoms
Finding
40
1
0.100
None
0
Microangiopathic hemolytic anemia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
31
0.100
None
0
Impaired cognition
disease
Mental Disorders
Mental or Behavioral Dysfunction
1630
348
0.100
None
0
Schistocytosis
phenotype
Laboratory or Test Result
5
0.100
None
0
Decreased serum complement factor I
phenotype
Finding
7
0.100
None
0
Decreased serum complement factor H
phenotype
Finding
4
0.100
None
0
Macular Degeneration, Age-Related, 1
disease
Eye Diseases
Disease or Syndrome
6
3
0.400
None
0
1
Macular drusen
phenotype
Eye Diseases
Finding
4
0.100
None
0
Serum creatinine raised
phenotype
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Finding
27
2
0.100
None
0
Dysphasia
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
63
4
0.100
None
0
Progressive visual loss
phenotype
Finding
77
11
0.100
None
0
Purpura
disease
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases
Disease or Syndrome
68
1
0.100
None
0
Complement deficiency disease
group
Immune System Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
42
0.300
moderate
0
Foveal hypopigmentation
phenotype
Finding
4
0.100
None
0
Hemiparesis
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
91
6
0.100
None
0
×
CUI:
C0015967
Disease:
Fever
Fever
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1021
66
0.100
None
0
Hyperlipidemia
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
472
83
0.100
None
0
Decreased serum complement factor B
phenotype
Finding
5
0.100
None
0
Diarrhea
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
632
63
0.100
None
0
Comatose
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
78
1
0.100
None
0