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: C0409326
Disease: Anterior knee pain
Anterior knee pain 		phenotype Sign or Symptom 1 0.010 None 1.000 1 2017 2017
CUI: C0596344
Disease: clinical anxiety
clinical anxiety 		disease Mental Disorders Mental or Behavioral Dysfunction 1 0.010 None 1.000 1 2017 2017
CUI: C1839455
Disease: Properdin Deficiency, Type II
Properdin Deficiency, Type II 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 1 1 0.100 None 0 1
CUI: C1839456
Disease: Properdin Deficiency, Type III
Properdin Deficiency, Type III 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 1 1 0.100 None 0 1
CUI: C1839458
Disease: Dysfunctional alternative complement pathway
Dysfunctional alternative complement pathway 		phenotype Finding 1 0.100 None 0
CUI: C1331541
Disease: Thymic Dysplasia
Thymic Dysplasia 		disease Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C2919706
Disease: Idiopathic rapidly progressive glomerulonephritis
Idiopathic rapidly progressive glomerulonephritis 		disease Disease or Syndrome 2 0.010 None 1.000 1 1984 1984
CUI: C1135745
Disease: Meningitis, Meningococcal, Serogroup A
Meningitis, Meningococcal, Serogroup A 		disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 2 1995 2000
CUI: C1135746
Disease: Meningitis, Meningococcal, Serogroup B
Meningitis, Meningococcal, Serogroup B 		disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 2 1995 2000
CUI: C1135747
Disease: Meningitis, Meningococcal, Serogroup C
Meningitis, Meningococcal, Serogroup C 		disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 2 1995 2000
CUI: C1136209
Disease: Meningitis, Meningococcal, Serogroup Y
Meningitis, Meningococcal, Serogroup Y 		disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 2 1995 2000
CUI: C1136210
Disease: Meningitis, Meningococcal, Serogroup W-135
Meningitis, Meningococcal, Serogroup W-135 		disease Infections; Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 2 1995 2000
CUI: C0398762
Disease: Properdin deficiency disease
Properdin deficiency disease 		disease Disease or Syndrome 4 0.510 strong 1.000 3 1980 2006
CUI: C0349251
Disease: Behavioral syndrome associated with physiological disturbance and physical factors
Behavioral syndrome associated with physiological disturbance and physical factors 		disease Mental Disorders Mental or Behavioral Dysfunction 8 2 0.010 None 1.000 1 2017 2017
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: C0233762
Disease: Hallucinations, Auditory
Hallucinations, Auditory 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Sign or Symptom 14 4 0.010 None 1.000 1 2017 2017
CUI: C4087273
Disease: C3 glomerulopathy
C3 glomerulopathy 		disease Disease or Syndrome 16 1 0.020 None 1.000 2 2017 2018
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: C0016065
Disease: Polyostotic fibrous dysplasia
Polyostotic fibrous dysplasia 		disease Musculoskeletal Diseases Congenital Abnormality 18 2 0.010 None 1.000 1 2019 2019
CUI: C0221239
Disease: Rapidly progressive glomerulonephritis
Rapidly progressive glomerulonephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 19 1 0.010 None 1.000 1 1984 1984
CUI: C0020624
Disease: Hypomenorrhea
Hypomenorrhea 		phenotype Pathological Conditions, Signs and Symptoms Disease or Syndrome 20 2 0.010 None 1.000 1 2017 2017
CUI: C0268647
Disease: Lysinuric Protein Intolerance
Lysinuric Protein Intolerance 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 21 47 0.010 None 1.000 1 2013 2013
CUI: C0233477
Disease: Dysphoric mood
Dysphoric mood 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 22 6 0.010 None 1.000 1 2018 2018
CUI: C0240602
Disease: opioid use
opioid use 		disease Mental or Behavioral Dysfunction 39 5 0.010 None 1.000 1 2019 2019
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease 		group Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 42 0.300 strong 1.000 1 1980 1980