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: C0035012
Disease: Reiter Syndrome
Reiter Syndrome 		disease Infections; Musculoskeletal Diseases Disease or Syndrome 14 0.010 None 1.000 1 1990 1990
CUI: C0949691
Disease: Spondylarthropathies
Spondylarthropathies 		group Musculoskeletal Diseases Disease or Syndrome 92 7 0.010 None 1.000 1 1990 1990
CUI: C0023470
Disease: Myeloid Leukemia
Myeloid Leukemia 		disease Neoplasms Neoplastic Process 385 7 0.010 None 1.000 1 1993 1993
CUI: C0085435
Disease: Arthritis, Reactive
Arthritis, Reactive 		disease Infections; Musculoskeletal Diseases Disease or Syndrome 63 2 0.010 None 1.000 1 1993 1993
CUI: C0424605
Disease: Developmental delay (disorder)
Developmental delay (disorder) 		phenotype Mental Disorders Mental or Behavioral Dysfunction 584 68 0.010 None 1.000 1 1996 1996
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease Mental or Behavioral Dysfunction 1825 553 0.010 None 1.000 1 1996 1996
CUI: C0085786
Disease: Hamman-Rich syndrome
Hamman-Rich syndrome 		disease Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases Disease or Syndrome 55 8 0.010 None 1.000 1 1998 1998
CUI: C0263680
Disease: Chronic arthritis
Chronic arthritis 		disease Musculoskeletal Diseases Disease or Syndrome 30 1 0.010 None 1.000 1 1998 1998
CUI: C2363866
Disease: Traumatic occlusion
Traumatic occlusion 		disease Disease or Syndrome 15 0.010 None 1.000 1 1998 1998
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 1998 1998
CUI: C0033036
Disease: Atrial Premature Complexes
Atrial Premature Complexes 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 183 21 0.020 None 1.000 2 1997 1999
CUI: C0346627
Disease: Intestinal Cancer
Intestinal Cancer 		disease Digestive System Diseases; Neoplasms Neoplastic Process 89 0.020 None 1.000 2 1997 1999
CUI: C0014072
Disease: Experimental Autoimmune Encephalomyelitis
Experimental Autoimmune Encephalomyelitis 		disease Immune System Diseases; Nervous System Diseases Experimental Model of Disease 97 0.200 None 1.000 1 1999 1999
CUI: C0019189
Disease: Hepatitis, Chronic
Hepatitis, Chronic 		disease Digestive System Diseases Disease or Syndrome 224 10 0.010 None 1.000 1 1999 1999
CUI: C0205696
Disease: Anaplastic carcinoma
Anaplastic carcinoma 		disease Neoplasms Neoplastic Process 232 3 0.300 None 1.000 1 1999 1999
CUI: C0205697
Disease: Carcinoma, Spindle-Cell
Carcinoma, Spindle-Cell 		disease Neoplasms Neoplastic Process 218 5 0.300 None 1.000 1 1999 1999
CUI: C0205699
Disease: Carcinomatosis
Carcinomatosis 		phenotype Neoplasms Neoplastic Process 186 2 0.300 None 1.000 1 1999 1999
CUI: C0206726
Disease: gliosarcoma
gliosarcoma 		disease Neoplasms Neoplastic Process 80 5 0.200 None 1.000 1 1999 1999
CUI: C0268237
Disease: Cytochrome-c Oxidase Deficiency
Cytochrome-c Oxidase Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome; Congenital Abnormality 65 44 0.010 None 1.000 1 1999 1999
CUI: C0747742
Disease: polyp benign
polyp benign 		disease Disease or Syndrome 10 0.010 None 1.000 1 1999 1999
CUI: C1514422
Disease: Glioblastoma, IDH-Wildtype
Glioblastoma, IDH-Wildtype 		disease Neoplasms Neoplastic Process 75 4 0.200 None 1.000 1 1999 1999
CUI: C2020625
Disease: Group B Streptococcal Infection
Group B Streptococcal Infection 		disease Infections Disease or Syndrome 55 0.010 None 1.000 1 1999 1999
CUI: C4083008
Disease: Guillain-Barre Syndrome, Familial
Guillain-Barre Syndrome, Familial 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 54 0.010 None 1.000 1 1999 1999
CUI: C0013221
Disease: Drug toxicity
Drug toxicity 		group Chemically-Induced Disorders Injury or Poisoning 86 0.300 None 1.000 1 2000 2000
CUI: C0027697
Disease: Nephritis
Nephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 296 40 0.010 None 1.000 1 2000 2000