C9, complement C9, 735

N. diseases: 62; N. variants: 32
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: C0015456
Disease: Facial Dermatoses
Facial Dermatoses
disease Skin and Connective Tissue Diseases Disease or Syndrome 1 0.300 None 1.000 1 2001 2001
CUI: C0343097
Disease: Nodular Elastoidosis
Nodular Elastoidosis
disease Skin and Connective Tissue Diseases Disease or Syndrome 1 0.300 None 1.000 1 2001 2001
MACULAR DEGENERATION, AGE-RELATED, 15
disease Disease or Syndrome 1 1 0.600 None 1.000 1 1 2013 2013
CUI: C4021093
Disease: Decreased serum complement C9
Decreased serum complement C9
phenotype Finding 1 0.100 None 0
CUI: C3151189
Disease: C9 Deficiency
C9 Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 2 5 0.750 strong 1.000 8 5 1998 2017
CUI: C0015704
Disease: Favre-Racouchot Syndrome
Favre-Racouchot Syndrome
disease Skin and Connective Tissue Diseases Disease or Syndrome 2 0.300 None 1.000 1 2001 2001
Meningitis, Meningococcal, Serogroup A
disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 1 1998 1998
Meningitis, Meningococcal, Serogroup B
disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 1 1998 1998
Meningitis, Meningococcal, Serogroup C
disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 1 1998 1998
Meningitis, Meningococcal, Serogroup Y
disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 1 1998 1998
Meningitis, Meningococcal, Serogroup W-135
disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 1 1998 1998
CUI: C0524661
Disease: Narcotic Abuse
Narcotic Abuse
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 6 0.300 None 1.000 1 2008 2008
CUI: C1527402
Disease: Narcotic Dependence
Narcotic Dependence
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 7 1 0.300 None 1.000 1 2008 2008
CUI: C0027412
Disease: Opioid-Related Disorders
Opioid-Related Disorders
group Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 12 23 0.300 None 1.000 1 2008 2008
CUI: C4551628
Disease: Opiate Abuse
Opiate Abuse
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 12 0.300 None 1.000 1 2008 2008
CUI: C0029095
Disease: Opioid abuse
Opioid abuse
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 16 0.300 None 1.000 1 2008 2008
CUI: C0025294
Disease: Meningococcal meningitis
Meningococcal meningitis
disease Infections; Nervous System Diseases Disease or Syndrome 17 3 0.300 None 1.000 1 1998 1998
CUI: C0003257
Disease: Antibody Deficiency Syndrome
Antibody Deficiency Syndrome
disease Immune System Diseases Disease or Syndrome 21 0.300 None 1.000 2 1998 2001
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease
group Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 42 0.310 strong 1.000 2 1998 1999
CUI: C2237660
Disease: exudative macular degeneration
exudative macular degeneration
disease Eye Diseases Disease or Syndrome 49 69 0.100 None 1.000 1 1 2016 2016
CUI: C0266526
Disease: Norrie disease
Norrie disease
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases Congenital Abnormality 55 28 0.010 None 1.000 1 2000 2000
Aspartate aminotransferase measurement
phenotype Laboratory Procedure 57 76 0.100 None 1.000 1 1 2018 2018
CUI: C0263666
Disease: Dermatomyositis, Childhood Type
Dermatomyositis, Childhood Type
disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 62 1 0.300 None 1.000 1 2001 2001
CUI: C0524662
Disease: Opiate Addiction
Opiate Addiction
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 81 46 0.300 None 1.000 1 2008 2008
CUI: C1536085
Disease: Geographic Atrophy
Geographic Atrophy
disease Eye Diseases Disease or Syndrome 85 81 0.100 None 1.000 1 1 2016 2016