PLA2G7, phospholipase A2 group VII, 7941

N. diseases: 136; N. variants: 11
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: C3280315
Disease: Platelet-Activating Factor Acetylhydrolase Deficiency
Platelet-Activating Factor Acetylhydrolase Deficiency 		disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 1 3 0.700 None 1.000 5 3 1996 1998
CUI: C4016754
Disease: ASTHMA AND ATOPY, SUSCEPTIBILITY TO
ASTHMA AND ATOPY, SUSCEPTIBILITY TO 		phenotype Finding 1 2 0.100 None 0 2
CUI: C4073143
Disease: Increased level of platelet-activating factor
Increased level of platelet-activating factor 		phenotype Finding 1 0.100 None 0
CUI: C1504438
Disease: Cerebral artery stenosis
Cerebral artery stenosis 		disease Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C4304667
Disease: Benign concentric annular macular dystrophy
Benign concentric annular macular dystrophy 		disease Disease or Syndrome 3 0.010 None 1.000 1 2008 2008
CUI: C2242539
Disease: Subcutaneous infection
Subcutaneous infection 		disease Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C1840253
Disease: IgE RESPONSIVENESS, ATOPIC
IgE RESPONSIVENESS, ATOPIC 		disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 5 0.300 None 0
CUI: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome 		disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 6 3 0.020 None 1.000 2 2014 2017
CUI: C3711850
Disease: Opticospinal Multiple Sclerosis
Opticospinal Multiple Sclerosis 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 7 0.010 None < 0.001 1 2004 2004
CUI: C1862596
Disease: Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia 		disease Nutritional and Metabolic Diseases Disease or Syndrome 12 24 0.010 None 1.000 1 1997 1997
CUI: C0543822
Disease: Atherosclerotic occlusive disease
Atherosclerotic occlusive disease 		disease Cardiovascular Diseases Disease or Syndrome 13 0.010 None 1.000 1 2000 2000
CUI: C0020523
Disease: Immediate hypersensitivity
Immediate hypersensitivity 		phenotype Immune System Diseases Pathologic Function 14 0.300 None 1.000 1 2000 2000
CUI: C4699508
Disease: Cardioembolism (high-risk/medium-risk)
Cardioembolism (high-risk/medium-risk) 		disease Disease or Syndrome 16 4 0.010 None 1.000 1 2017 2017
CUI: C4700045
Disease: Non-ST-segment elevation myocardial infarction (NSTEMI)
Non-ST-segment elevation myocardial infarction (NSTEMI) 		disease Disease or Syndrome 18 1 0.010 None 1.000 1 2019 2019
CUI: C0020597
Disease: Hypobetalipoproteinemias
Hypobetalipoproteinemias 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 20 11 0.010 None 1.000 1 1997 1997
CUI: C0010073
Disease: Coronary Artery Vasospasm
Coronary Artery Vasospasm 		disease Cardiovascular Diseases Disease or Syndrome 30 9 0.010 None 1.000 1 1 2002 2002
CUI: C1306889
Disease: Peripheral arterial occlusive disease
Peripheral arterial occlusive disease 		disease Cardiovascular Diseases Disease or Syndrome 35 3 0.010 None 1.000 1 2006 2006
CUI: C0403396
Disease: Steroid-sensitive nephrotic syndrome
Steroid-sensitive nephrotic syndrome 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 36 11 0.010 None 1.000 1 1998 1998
CUI: C0004606
Disease: Nonproliferative diabetic retinopathy
Nonproliferative diabetic retinopathy 		disease Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 41 1 0.010 None 1.000 1 2017 2017
CUI: C0751633
Disease: Carotid Artery Plaque
Carotid Artery Plaque 		disease Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 41 3 0.010 None 1.000 1 2017 2017
CUI: C0342882
Disease: Familial hypercholesterolemia - heterozygous
Familial hypercholesterolemia - heterozygous 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 42 34 0.020 None 1.000 2 1997 2011
CUI: C4699512
Disease: Large-artery atherosclerosis (embolus/thrombosis)
Large-artery atherosclerosis (embolus/thrombosis) 		disease Disease or Syndrome 48 35 0.010 None 1.000 1 2017 2017
CUI: C1257915
Disease: Intestinal Polyposis
Intestinal Polyposis 		disease Digestive System Diseases Disease or Syndrome 49 3 0.010 None 1.000 1 2013 2013
CUI: C4699152
Disease: ST-segment elevation myocardial infarction (STEMI)
ST-segment elevation myocardial infarction (STEMI) 		disease Disease or Syndrome 51 2 0.010 None 1.000 1 2019 2019
CUI: C1260873
Disease: Aortic valve disorder
Aortic valve disorder 		disease Cardiovascular Diseases Disease or Syndrome 58 0.010 None 1.000 1 2014 2014