C1QA, complement C1q A chain, 712

N. diseases: 88; N. variants: 5
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C3150902
Disease: C1q DEFICIENCY
C1q DEFICIENCY
disease Disease or Syndrome 5 8 0.610 strong 1.000 2 2 2012 2017
CUI: C3280742
Disease: SYSTEMIC LUPUS ERYTHEMATOSUS 16
SYSTEMIC LUPUS ERYTHEMATOSUS 16
disease Disease or Syndrome 5 0.300 None 1.000 1 2004 2004
CUI: C1142517
Disease: Lupus anticoagulant measurement
Lupus anticoagulant measurement
phenotype Laboratory Procedure 5 0.100 None 0
CUI: C4073169
Disease: Decreased serum complement C4
Decreased serum complement C4
phenotype Finding 5 0.100 None 0
CUI: C4321325
Disease: Lupus anticoagulant -- finding
Lupus anticoagulant -- finding
phenotype Finding 5 0.100 None 0
Membranoproliferative Glomerulonephritis, Type III
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 6 0.300 None 1.000 1 1996 1996
CUI: C0426396
Disease: Urine looks dark
Urine looks dark
phenotype Finding 6 0.100 None 0
Membranoproliferative Glomerulonephritis, Type I
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 7 0.300 None 1.000 1 1996 1996
CUI: C1970257
Disease: Decreased serum complement factor I
Decreased serum complement factor I
phenotype Finding 7 0.100 None 0
CUI: C3805247
Disease: Late onset neutropenia
Late onset neutropenia
disease Hemic and Lymphatic Diseases Disease or Syndrome 9 3 0.010 None 1.000 1 1 2012 2012
CUI: C0020951
Disease: Immune Complex Diseases
Immune Complex Diseases
group Immune System Diseases Disease or Syndrome 10 0.300 None 1.000 1 1996 1996
Membranoproliferative Glomerulonephritis, Type II
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 10 3 0.300 None 1.000 1 1996 1996
CUI: C1837512
Disease: Decreased serum complement C3
Decreased serum complement C3
phenotype Finding 12 0.100 None 0
Other specified iron deficiency anemias
disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 13 0.200 None 1.000 1 2008 2008
CUI: C0277942
Disease: Butterfly rash
Butterfly rash
phenotype Skin and Connective Tissue Diseases Finding 13 0.100 None 0
Abnormality of the gastrointestinal tract
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Anatomical Abnormality 14 1 0.100 None 0
CUI: C1858981
Disease: Antineutrophil antibody positivity
Antineutrophil antibody positivity
phenotype Laboratory or Test Result 15 0.100 None 0
Antiphospholipid antibody positivity
phenotype Finding 18 0.100 None 0
Increased lactate dehydrogenase activity
phenotype Finding 27 0.100 None 0
CUI: C0221021
Disease: Microangiopathic hemolytic anemia
Microangiopathic hemolytic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 31 0.100 None 0
CUI: C0151480
Disease: Anti-nuclear factor positive
Anti-nuclear factor positive
phenotype Skin and Connective Tissue Diseases Laboratory or Test Result 35 3 0.100 None 0
CUI: C0234428
Disease: Disturbance of consciousness
Disturbance of consciousness
phenotype Finding 35 0.100 None 0
CUI: C0151632
Disease: ESR raised
ESR raised
phenotype Finding 36 0.100 None 0
CUI: C0024137
Disease: Lupus Erythematosus, Cutaneous
Lupus Erythematosus, Cutaneous
disease Skin and Connective Tissue Diseases Disease or Syndrome 39 7 0.010 None 1.000 1 2003 2003
Lupus Erythematosus, Subacute Cutaneous
disease Skin and Connective Tissue Diseases Disease or Syndrome 39 1 0.010 None 1.000 1 2003 2003