PTAFR, platelet activating factor receptor, 5724

N. diseases: 96; N. variants: 6
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: C0036986
Disease: Shock, Traumatic
Shock, Traumatic
phenotype Pathological Conditions, Signs and Symptoms; Wounds and Injuries Pathologic Function 1 0.200 None 1.000 1 1990 1990
CUI: C4551465
Disease: Small airways disease
Small airways disease
disease Disease or Syndrome 4 0.010 None 1.000 1 2016 2016
CUI: C0339808
Disease: House dust mite allergy
House dust mite allergy
phenotype Pathological Conditions, Signs and Symptoms; Infections; Immune System Diseases Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome
disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 6 3 0.010 None 1.000 1 2 2017 2017
CUI: C0151683
Disease: Neutrophilia (finding)
Neutrophilia (finding)
phenotype Finding 6 1 0.200 None 1.000 1 2000 2000
Other specified forms of pleural effusion, except tuberculous
disease Infections; Respiratory Tract Diseases Disease or Syndrome 15 0.200 None 1.000 1 1993 1993
CUI: C0025205
Disease: Melanoma, Experimental
Melanoma, Experimental
disease Neoplasms Neoplastic Process; Experimental Model of Disease 25 0.010 None 1.000 1 2017 2017
CUI: C0026766
Disease: Multiple Organ Failure
Multiple Organ Failure
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 25 0.200 None 1.000 1 1998 1998
CUI: C1096293
Disease: Macroangiopathy
Macroangiopathy
disease Disease or Syndrome 31 6 0.010 None 1.000 1 2018 2018
CUI: C0206620
Disease: Lymphangioma, Cystic
Lymphangioma, Cystic
disease Neoplasms Neoplastic Process 43 1 0.010 None 1.000 1 2017 2017
CUI: C0262405
Disease: Cerebral dysfunction
Cerebral dysfunction
disease Nervous System Diseases Disease or Syndrome 45 0.010 None 1.000 1 2017 2017
Invasive Streptococcus pneumoniae disease
disease Infections Disease or Syndrome 55 9 0.020 None 1.000 2 2011 2013
CUI: C0266463
Disease: Lissencephaly
Lissencephaly
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 71 9 0.010 None 1.000 1 2006 2006
CUI: C0596321
Disease: Chemical Carcinogenesis
Chemical Carcinogenesis
phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 71 2 0.010 None 1.000 1 2018 2018
CUI: C0009763
Disease: Conjunctivitis
Conjunctivitis
disease Eye Diseases Disease or Syndrome 82 1 0.200 None 1.000 1 2005 2005
CUI: C0032269
Disease: Pneumococcal Infections
Pneumococcal Infections
group Infections Disease or Syndrome 85 1 0.030 None 1.000 3 2013 2017
CUI: C0155862
Disease: Streptococcal pneumonia
Streptococcal pneumonia
disease Infections; Respiratory Tract Diseases Disease or Syndrome 100 2 0.030 None 1.000 3 2012 2016
CUI: C0520459
Disease: Necrotizing Enterocolitis
Necrotizing Enterocolitis
disease Digestive System Diseases Disease or Syndrome 103 7 0.200 None 1.000 1 2007 2007
CUI: C0149940
Disease: Sciatic Neuropathy
Sciatic Neuropathy
disease Nervous System Diseases Disease or Syndrome 115 0.200 None 1.000 1 2012 2012
Disseminated Intravascular Coagulation
disease Hemic and Lymphatic Diseases Disease or Syndrome 117 3 0.010 None 1.000 1 2019 2019
CUI: C0085109
Disease: Corneal Neovascularization
Corneal Neovascularization
disease Pathological Conditions, Signs and Symptoms; Eye Diseases Disease or Syndrome 117 0.010 None 1.000 1 2015 2015
CUI: C1456781
Disease: Benign melanocytic nevus
Benign melanocytic nevus
disease Neoplasms Neoplastic Process 122 20 0.010 None 1.000 1 2018 2018
CUI: C0020649
Disease: Hypotension
Hypotension
phenotype Cardiovascular Diseases Finding 125 2 0.200 None 1.000 1 1986 1986
CUI: C0018498
Disease: Hair Color
Hair Color
phenotype Organism Attribute 130 312 0.100 None 1.000 1 1 2018 2018
CUI: C0699893
Disease: Skin carcinoma
Skin carcinoma
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 136 24 0.010 None 1.000 1 2018 2018