C1QB, complement C1q B chain, 713

N. diseases: 9; N. variants: 5
Source: BEFREE ×
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 4 0.710 strong 1.000 1 1997 2015
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 1686 635 0.320 strong 1.000 2 2 2002 2013
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
disease Mental Disorders Mental or Behavioral Dysfunction 2217 1332 0.310 None 1.000 1 3 2011 2011
CUI: C0002726
Disease: Amyloidosis
Amyloidosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 685 93 0.010 None 1.000 1 2019 2019
CUI: C0025202
Disease: melanoma
melanoma
disease Neoplasms Neoplastic Process 2890 352 0.010 None 1.000 1 2011 2011
CUI: C0027796
Disease: Neuralgia
Neuralgia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 755 16 0.010 None 1.000 1 2018 2018
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 228 54 0.010 None 1.000 1 2016 2016
CUI: C0206138
Disease: CREST Syndrome
CREST Syndrome
disease Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 54 6 0.010 None 1.000 1 2015 2015
Amyotrophic Lateral Sclerosis, Sporadic
disease Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 111 43 0.010 None 1.000 1 1999 1999