CFP, complement factor properdin, 5199

N. diseases: 108; N. variants: 7
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: C0016065
Disease: Polyostotic fibrous dysplasia
Polyostotic fibrous dysplasia
disease Musculoskeletal Diseases Congenital Abnormality 18 2 0.010 None 1.000 1 2019 2019
CUI: C0259779
Disease: Fibrous Dysplasia
Fibrous Dysplasia
disease Congenital Abnormality 53 5 0.010 None 1.000 1 2019 2019
Progressive pseudorheumatoid dysplasia
disease Musculoskeletal Diseases Congenital Abnormality 64 27 0.010 None 1.000 1 2017 2017
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
disease Infections Disease or Syndrome 1256 328 0.100 None 1.000 39 2000 2019
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary
disease Infections; Respiratory Tract Diseases Disease or Syndrome 358 171 0.090 None 1.000 9 2009 2019
CUI: C1839454
Disease: PROPERDIN DEFICIENCY, X-LINKED
PROPERDIN DEFICIENCY, X-LINKED
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 11 5 0.700 limited 1.000 7 5 1995 2019
CUI: C1609538
Disease: Latent Tuberculosis
Latent Tuberculosis
disease Infections Disease or Syndrome 183 18 0.050 None 1.000 5 2004 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
disease Nervous System Diseases Disease or Syndrome 2078 990 0.030 None 1.000 3 2010 2019
CUI: C0041326
Disease: Pleural Tuberculosis
Pleural Tuberculosis
disease Infections; Respiratory Tract Diseases Disease or Syndrome 59 0.030 None 1.000 3 2011 2019
CUI: C0151332
Disease: Active tuberculosis
Active tuberculosis
disease Infections Disease or Syndrome 116 25 0.030 None 1.000 3 2012 2017
CUI: C0398762
Disease: Properdin deficiency disease
Properdin deficiency disease
disease Disease or Syndrome 4 0.510 strong 1.000 3 1980 2006
CUI: C0023343
Disease: Leprosy
Leprosy
disease Infections Disease or Syndrome 190 120 0.020 None 1.000 2 2004 2006
CUI: C0025294
Disease: Meningococcal meningitis
Meningococcal meningitis
disease Infections; Nervous System Diseases Disease or Syndrome 17 3 0.300 None 1.000 2 1995 2000
CUI: C0025303
Disease: Meningococcal Infections
Meningococcal Infections
group Infections Disease or Syndrome 69 32 0.020 None 1.000 2 1998 1999
CUI: C0162429
Disease: Malnutrition
Malnutrition
disease Nutritional and Metabolic Diseases Disease or Syndrome 417 29 0.020 None 1.000 2 1989 2019
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
disease Eye Diseases Disease or Syndrome 685 663 0.020 None 0.500 2 1 2010 2012
CUI: C0679362
Disease: Tuberculosis, extrapulmonary
Tuberculosis, extrapulmonary
disease Infections Disease or Syndrome 58 21 0.020 None 1.000 2 2016 2019
Meningitis, Meningococcal, Serogroup A
disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 2 1995 2000
Meningitis, Meningococcal, Serogroup B
disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 2 1995 2000
Meningitis, Meningococcal, Serogroup C
disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 2 1995 2000
Meningitis, Meningococcal, Serogroup Y
disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 2 1995 2000
Meningitis, Meningococcal, Serogroup W-135
disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 2 1995 2000
CUI: C1318485
Disease: Liver regeneration disorder
Liver regeneration disorder
phenotype Digestive System Diseases Disease or Syndrome 346 0.020 None 1.000 2 2019 2019
CUI: C4087273
Disease: C3 glomerulopathy
C3 glomerulopathy
disease Disease or Syndrome 16 1 0.020 None 1.000 2 2017 2018
CUI: C0011603
Disease: Dermatitis
Dermatitis
disease Skin and Connective Tissue Diseases Disease or Syndrome 496 16 0.010 None 1.000 1 2019 2019