PLA2G15, phospholipase A2 group XV, 23659

N. diseases: 170; 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: C0311269
Disease: Irreducible ventral hernia
Irreducible ventral hernia 		phenotype Pathological Conditions, Signs and Symptoms Acquired Abnormality 3 0.010 None 1.000 1 2019 2019
CUI: C0375553
Disease: Continuous leakage of urine
Continuous leakage of urine 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Sign or Symptom 3 0.010 None 1.000 1 2017 2017
CUI: C4546318
Disease: Organ surgical site infection
Organ surgical site infection 		disease Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C0010046
Disease: Corn of toe
Corn of toe 		disease Skin and Connective Tissue Diseases Acquired Abnormality 4 0.010 None 1.000 1 1997 1997
CUI: C2609176
Disease: Kounis Syndrome
Kounis Syndrome 		disease Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C0042582
Disease: Vesicovaginal Fistula
Vesicovaginal Fistula 		disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C0410698
Disease: Neuromuscular scoliosis
Neuromuscular scoliosis 		disease Musculoskeletal Diseases Disease or Syndrome 5 0.010 None 1.000 1 2019 2019
CUI: C0267725
Disease: Paraesophageal hernia
Paraesophageal hernia 		phenotype Pathological Conditions, Signs and Symptoms Disease or Syndrome 7 0.010 None 1.000 1 2018 2018
CUI: C0585129
Disease: Retroperitoneal sarcoma
Retroperitoneal sarcoma 		disease Neoplasms Neoplastic Process 8 0.010 None 1.000 1 2019 2019
CUI: C0854119
Disease: Ruptured Appendicitis
Ruptured Appendicitis 		disease Digestive System Diseases; Infections Disease or Syndrome 9 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 0.010 None 1.000 1 2019 2019
CUI: C1852540
Disease: Coronary Artery Dissection, Spontaneous
Coronary Artery Dissection, Spontaneous 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 11 0.010 None 1.000 1 2019 2019
CUI: C3160886
Disease: Non ST segment elevation acute coronary syndrome
Non ST segment elevation acute coronary syndrome 		disease Disease or Syndrome 12 2 0.020 None 1.000 2 2017 2019
CUI: C0701818
Disease: Choledocholithiasis
Choledocholithiasis 		disease Digestive System Diseases Disease or Syndrome 12 0.010 None 1.000 1 2019 2019
CUI: C0086447
Disease: Ileal Pouches
Ileal Pouches 		disease Acquired Abnormality 13 0.010 None 1.000 1 2018 2018
CUI: C0037939
Disease: Spinal Neoplasms
Spinal Neoplasms 		group Neoplasms; Musculoskeletal Diseases Neoplastic Process 14 0.010 None 1.000 1 2018 2018
CUI: C3887662
Disease: Intraspinal Neoplasm
Intraspinal Neoplasm 		disease Neoplasms; Musculoskeletal Diseases; Nervous System Diseases Neoplastic Process 14 0.010 None 1.000 1 2018 2018
CUI: C0038017
Disease: Congenital spondylolisthesis
Congenital spondylolisthesis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 17 1 0.010 None 1.000 1 2018 2018
CUI: C1561921
Disease: Non-ST elevation (NSTEMI) myocardial infarction
Non-ST elevation (NSTEMI) myocardial infarction 		disease Disease or Syndrome 17 0.010 None 1.000 1 2017 2017
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: C0014852
Disease: Esophageal Diseases
Esophageal Diseases 		group Digestive System Diseases Disease or Syndrome 19 1 0.010 None 1.000 1 2018 2018
CUI: C0149520
Disease: Acute Cholecystitis
Acute Cholecystitis 		disease Digestive System Diseases Disease or Syndrome 21 0.020 None 1.000 2 2017 2019
CUI: C4290140
Disease: recurrent myocardial infarction
recurrent myocardial infarction 		disease Disease or Syndrome 22 6 0.010 None 1.000 1 2018 2018
CUI: C0878552
Disease: Coronary artery ectasia
Coronary artery ectasia 		disease Disease or Syndrome 24 1 0.010 None 1.000 1 2019 2019
CUI: C0019322
Disease: Umbilical hernia
Umbilical hernia 		phenotype Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 27 17 0.010 None 1.000 1 2017 2017