PLA2G2A, phospholipase A2 group IIA, 5320

N. diseases: 215; 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: C1868001
Disease: Polyposis Of Gastric Fundus Without Polyposis Coli
Polyposis Of Gastric Fundus Without Polyposis Coli 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Neoplasms Neoplastic Process 4 1 0.010 None < 0.001 1 2007 2007
CUI: C0578477
Disease: Duodenal polyposis
Duodenal polyposis 		disease Neoplastic Process 5 2 0.010 None < 0.001 1 1996 1996
CUI: C1868251
Disease: Neonatal alloimmune thrombocytopenia (NAIT)
Neonatal alloimmune thrombocytopenia (NAIT) 		disease Disease or Syndrome 6 0.010 None 1.000 1 1994 1994
CUI: C0850572
Disease: Adenomatous polyp of colon
Adenomatous polyp of colon 		disease Pathological Conditions, Signs and Symptoms Neoplastic Process 7 3 0.010 None 1.000 1 1996 1996
CUI: C1260881
Disease: Allergic bronchitis
Allergic bronchitis 		disease Infections; Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 8 2 0.010 None 1.000 1 2013 2013
CUI: C2674616
Disease: FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder)
FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms Disease or Syndrome 10 7 0.010 None < 0.001 1 1996 1996
CUI: C0270500
Disease: Coprophilia (disorder)
Coprophilia (disorder) 		disease Mental Disorders Mental or Behavioral Dysfunction 12 0.010 None 1.000 1 2014 2014
CUI: C0221028
Disease: Neonatal thrombocytopenia (disorder)
Neonatal thrombocytopenia (disorder) 		disease Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 15 2 0.010 None 1.000 1 1994 1994
CUI: C1840061
Disease: SMALL PATELLA SYNDROME
SMALL PATELLA SYNDROME 		disease Musculoskeletal Diseases Disease or Syndrome 21 15 0.010 None 1.000 1 2014 2014
CUI: C0311361
Disease: Adenomatous goiter
Adenomatous goiter 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 23 4 0.010 None 1.000 1 2005 2005
CUI: C1260403
Disease: prothrombin gene mutation
prothrombin gene mutation 		phenotype Hemic and Lymphatic Diseases Disease or Syndrome 23 5 0.010 None 1.000 1 2008 2008
CUI: C2350019
Disease: Solitary Pulmonary Nodule
Solitary Pulmonary Nodule 		disease Respiratory Tract Diseases Neoplastic Process 25 0.010 None 1.000 1 2018 2018
CUI: C0262929
Disease: Myxoma of the Endocardium
Myxoma of the Endocardium 		disease Neoplasms Neoplastic Process 28 0.010 None 1.000 1 2004 2004
CUI: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 29 1 0.060 None 1.000 6 1992 2006
CUI: C0349218
Disease: Recurrent depressive disorder
Recurrent depressive disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 29 9 0.310 None 1.000 1 2012 2012
CUI: C0039292
Disease: Tangier Disease
Tangier Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 31 28 0.010 None 1.000 1 2007 2007
CUI: C0085292
Disease: Stiff-Person Syndrome
Stiff-Person Syndrome 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 34 9 0.010 None 1.000 1 2014 2014
CUI: C0598428
Disease: genetic hypertension
genetic hypertension 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 34 2 0.010 None < 0.001 1 1999 1999
CUI: C0010072
Disease: Coronary Thrombosis
Coronary Thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 35 2 0.040 None 1.000 4 1996 2005
CUI: C0154841
Disease: Central retinal vein occlusion
Central retinal vein occlusion 		disease Eye Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 38 7 0.010 None 1.000 1 1999 1999
CUI: C0684256
Disease: Bacterial sepsis
Bacterial sepsis 		disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 38 0.010 None 1.000 1 2018 2018
CUI: C0272285
Disease: Heparin-induced thrombocytopenia
Heparin-induced thrombocytopenia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 44 5 0.010 None 1.000 1 2008 2008
CUI: C4049711
Disease: Lepidic Predominant Adenocarcinoma
Lepidic Predominant Adenocarcinoma 		disease Neoplasms Neoplastic Process 46 0.010 None 1.000 1 2015 2015
CUI: C0021846
Disease: Intestinal Polyps
Intestinal Polyps 		phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 48 1 0.010 None 1.000 1 1996 1996
CUI: C0040015
Disease: Thrombasthenia
Thrombasthenia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 48 61 0.010 None 1.000 1 1996 1996