P2RX7, purinergic receptor P2X 7, 5027

N. diseases: 337; N. variants: 23
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: C2242589
Disease: Coronaropathy
Coronaropathy
disease Disease or Syndrome 2 0.010 None 1.000 1 2013 2013
CUI: C2902981
Disease: Neurogenic bladder dysfunction
Neurogenic bladder dysfunction
disease Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C0028790
Disease: Cerebral artery occlusion
Cerebral artery occlusion
disease Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 9 0.010 None 1.000 1 2019 2019
CUI: C1864997
Disease: Majeed syndrome
Majeed syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections; Musculoskeletal Diseases; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 15 6 0.010 None 1.000 1 2018 2018
CUI: C0746402
Disease: manic symptom
manic symptom
phenotype Mental or Behavioral Dysfunction 16 1 0.010 None 1.000 1 2012 2012
CUI: C0159020
Disease: Convulsions in the newborn
Convulsions in the newborn
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 17 4 0.020 None 1.000 2 2016 2017
CUI: C1141926
Disease: Abdominal sepsis
Abdominal sepsis
disease Disease or Syndrome 18 0.010 None 1.000 1 2017 2017
CUI: C1719494
Disease: PERIODONTITIS, LOCALIZED AGGRESSIVE
PERIODONTITIS, LOCALIZED AGGRESSIVE
disease Stomatognathic Diseases Disease or Syndrome 20 2 0.010 None 1.000 1 1 2020 2020
THANATOPHORIC DYSPLASIA, TYPE I (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 20 18 0.010 None 1.000 1 2018 2018
CUI: C2936331
Disease: Sarcoglycanopathies
Sarcoglycanopathies
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 20 3 0.010 None 1.000 1 2019 2019
CUI: C3249881
Disease: Infection - suppurative
Infection - suppurative
group Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 20 0.010 None 1.000 1 2019 2019
CUI: C1281914
Disease: Corneal allograft rejection
Corneal allograft rejection
disease Disease or Syndrome 21 3 0.010 None 1.000 1 2019 2019
CUI: C1443892
Disease: Chronic Q Fever
Chronic Q Fever
disease Infections Disease or Syndrome 22 9 0.010 None 1.000 1 2 2019 2019
CUI: C0014558
Disease: Uncinate Epilepsy
Uncinate Epilepsy
disease Nervous System Diseases Disease or Syndrome 23 0.300 None 1.000 2 2002 2009
Epilepsy, Benign Psychomotor, Childhood
disease Nervous System Diseases Disease or Syndrome 23 0.300 None 1.000 2 2002 2009
CUI: C0085315
Disease: Toxoplasmosis, Cerebral
Toxoplasmosis, Cerebral
disease Infections; Nervous System Diseases Disease or Syndrome 23 0.010 None 1.000 1 2019 2019
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine
disease Nervous System Diseases Disease or Syndrome 24 17 0.010 None 1.000 1 2017 2017
CUI: C3178766
Disease: Nociceptive Pain
Nociceptive Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 25 0.010 None 1.000 1 2017 2017
CUI: C3887558
Disease: Hemophagocytic Syndrome
Hemophagocytic Syndrome
disease Hemic and Lymphatic Diseases Disease or Syndrome 25 3 0.010 None < 0.001 1 2012 2012
CUI: C0020630
Disease: Hypophosphatasia
Hypophosphatasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 27 29 0.300 None 1.000 1 2016 2016
CUI: C0393682
Disease: Epilepsy, Lateral Temporal
Epilepsy, Lateral Temporal
disease Nervous System Diseases Disease or Syndrome 29 1 0.300 None 1.000 2 2002 2009
CUI: C0001818
Disease: Agoraphobia
Agoraphobia
disease Mental Disorders Mental or Behavioral Dysfunction 29 11 0.010 None 1.000 1 1 2007 2007
CUI: C0041330
Disease: Tuberculosis, Spinal
Tuberculosis, Spinal
disease Infections; Musculoskeletal Diseases Disease or Syndrome 29 8 0.010 None 1.000 1 2018 2018
CUI: C0409980
Disease: Primary antiphospholipid syndrome
Primary antiphospholipid syndrome
disease Immune System Diseases Disease or Syndrome 29 1 0.010 None 1.000 1 2019 2019
CUI: C2718067
Disease: Alcoholic Steatohepatitis
Alcoholic Steatohepatitis
disease Digestive System Diseases; Chemically-Induced Disorders Disease or Syndrome 30 0.010 None 1.000 1 2018 2018