PTGS2, prostaglandin-endoperoxide synthase 2, 5743

N. diseases: 1234; N. variants: 27
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: C0740391
Disease: Middle Cerebral Artery Occlusion
Middle Cerebral Artery Occlusion
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 626 0.070 None 1.000 7 1999 2019
CUI: C1963943
Disease: Atherothrombosis
Atherothrombosis
disease Acquired Abnormality 115 15 0.060 None 1.000 6 2005 2014
CUI: C0333293
Disease: Healing ulcer
Healing ulcer
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 43 1 0.040 None 1.000 4 2001 2017
CUI: C0281899
Disease: Prolapsed lumbar disc
Prolapsed lumbar disc
disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Acquired Abnormality 75 33 0.030 None 1.000 3 2002 2017
CUI: C0376154
Disease: Skin callus
Skin callus
disease Skin and Connective Tissue Diseases Acquired Abnormality 154 0.020 None 1.000 2 2010 2018
CUI: C0001510
Disease: Postoperative adhesion
Postoperative adhesion
phenotype Pathological Conditions, Signs and Symptoms Acquired Abnormality 9 0.010 None 1.000 1 2003 2003
CUI: C0086447
Disease: Ileal Pouches
Ileal Pouches
disease Acquired Abnormality 13 0.010 None 1.000 1 2001 2001
CUI: C0086543
Disease: Cataract
Cataract
disease Eye Diseases Acquired Abnormality 878 124 0.010 None 1.000 1 2015 2015
CUI: C0162810
Disease: Cicatrix, Hypertrophic
Cicatrix, Hypertrophic
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 185 3 0.010 None 1.000 1 2017 2017
CUI: C0242362
Disease: Disk, Herniated
Disk, Herniated
disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Acquired Abnormality 31 0.010 None 1.000 1 2007 2007
Amputated structure (morphologic abnormality)
phenotype Wounds and Injuries Acquired Abnormality 94 0.010 None 1.000 1 2018 2018
CUI: C0332853
Disease: Anastomosis
Anastomosis
disease Acquired Abnormality 155 2 0.010 None 1.000 1 2015 2015
CUI: C0333294
Disease: Recurrent ulcer
Recurrent ulcer
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 3 0.010 None 1.000 1 2017 2017
CUI: C0333307
Disease: Superficial ulcer
Superficial ulcer
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 242 10 0.010 None 1.000 1 2001 2001
CUI: C0549357
Disease: Abdominal adhesions
Abdominal adhesions
disease Digestive System Diseases Acquired Abnormality 6 0.010 None 1.000 1 2015 2015
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 2002 2002
CUI: C1262048
Disease: Glial scar
Glial scar
phenotype Acquired Abnormality 51 0.010 None 1.000 1 2019 2019
CUI: C4477086
Disease: Cotton wool plaques
Cotton wool plaques
phenotype Pathological Conditions, Signs and Symptoms Acquired Abnormality 4 0.010 None 1.000 1 2003 2003
CUI: C0032584
Disease: polyps
polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 390 18 0.100 None 1.000 26 1999 2019
CUI: C0021846
Disease: Intestinal Polyps
Intestinal Polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 48 1 0.340 None 1.000 7 1998 2017
CUI: C0014511
Disease: Epithelial cyst
Epithelial cyst
phenotype Neoplasms Anatomical Abnormality 38 0.020 None 1.000 2 2003 2019
CUI: C0009376
Disease: Colonic Polyps
Colonic Polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 69 8 0.010 None 1.000 1 2016 2016
CUI: C0009918
Disease: Contracture of joint
Contracture of joint
disease Musculoskeletal Diseases Anatomical Abnormality 36 0.010 None 1.000 1 2019 2019
CUI: C0269155
Disease: Germinal inclusion cyst of ovary
Germinal inclusion cyst of ovary
disease Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Anatomical Abnormality 3 0.010 None 1.000 1 2003 2003
CUI: C1567435
Disease: Polycystic Kidney - body part
Polycystic Kidney - body part
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Anatomical Abnormality 54 1 0.010 None 1.000 1 2019 2019