BDKRB2, bradykinin receptor B2, 624

N. diseases: 105; N. variants: 7
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: C0015378
Disease: Extravasation of Contrast Media
Extravasation of Contrast Media
phenotype Pathological Conditions, Signs and Symptoms; Wounds and Injuries Pathologic Function 6 0.300 None 1.000 1 1998 1998
CUI: C0086457
Disease: Industrial Dermatosis
Industrial Dermatosis
disease Skin and Connective Tissue Diseases; Occupational Diseases Disease or Syndrome 8 0.300 None 1.000 1 2019 2019
CUI: C0028796
Disease: Dermatitis, Occupational
Dermatitis, Occupational
disease Skin and Connective Tissue Diseases; Occupational Diseases Disease or Syndrome 11 0.300 None 1.000 1 2019 2019
CUI: C0042484
Disease: Venous Engorgement
Venous Engorgement
phenotype Cardiovascular Diseases Pathologic Function 13 0.300 None 1.000 1 2002 2002
CUI: C0178824
Disease: Reactive Hyperemia
Reactive Hyperemia
phenotype Cardiovascular Diseases Pathologic Function 13 0.300 None 1.000 1 2002 2002
CUI: C0333233
Disease: Active Hyperemia
Active Hyperemia
phenotype Cardiovascular Diseases Pathologic Function 13 0.300 None 1.000 1 2002 2002
Other specified forms of pleural effusion, except tuberculous
disease Infections; Respiratory Tract Diseases Disease or Syndrome 15 0.200 None 1.000 1 1997 1997
CUI: C0238284
Disease: Acute mountain sickness
Acute mountain sickness
disease Respiratory Tract Diseases Disease or Syndrome 21 3 0.010 None 1.000 1 2010 2010
CUI: C0014558
Disease: Uncinate Epilepsy
Uncinate Epilepsy
disease Nervous System Diseases Disease or Syndrome 23 0.300 None 1.000 1 2004 2004
Epilepsy, Benign Psychomotor, Childhood
disease Nervous System Diseases Disease or Syndrome 23 0.300 None 1.000 1 2004 2004
CUI: C0393682
Disease: Epilepsy, Lateral Temporal
Epilepsy, Lateral Temporal
disease Nervous System Diseases Disease or Syndrome 29 1 0.300 None 1.000 1 2004 2004
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Stomatognathic Diseases Disease or Syndrome 41 14 0.010 None 1.000 1 1 2010 2010
CUI: C0087086
Disease: Thrombus
Thrombus
phenotype Cardiovascular Diseases Pathologic Function 46 0.300 None 1.000 1 2006 2006
CUI: C0019080
Disease: Hemorrhage
Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 47 0.300 None 1.000 1 2006 2006
CUI: C0234238
Disease: Ache
Ache
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.300 None 1.000 1 2010 2010
CUI: C0458257
Disease: Pain, Splitting
Pain, Splitting
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.300 None 1.000 1 2010 2010
CUI: C0458259
Disease: Pain, Crushing
Pain, Crushing
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.300 None 1.000 1 2010 2010
CUI: C0751407
Disease: Pain, Migratory
Pain, Migratory
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.300 None 1.000 1 2010 2010
CUI: C0751408
Disease: Suffering, Physical
Suffering, Physical
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.300 None 1.000 1 2010 2010
CUI: C0234254
Disease: Radiating pain
Radiating pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 51 0.300 None 1.000 1 2010 2010
CUI: C0019243
Disease: Angioedemas, Hereditary
Angioedemas, Hereditary
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 54 7 0.020 None 1.000 2 1994 1997
CUI: C0234230
Disease: Pain, Burning
Pain, Burning
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 56 0.300 None 1.000 1 2010 2010
CUI: C0020452
Disease: Hyperemia
Hyperemia
disease Cardiovascular Diseases Disease or Syndrome 64 3 0.300 None 1.000 1 2002 2002
CUI: C0458247
Disease: Allodynia
Allodynia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 84 0.300 None 1.000 3 2008 2010
CUI: C0751211
Disease: Hyperalgesia, Primary
Hyperalgesia, Primary
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 84 0.300 None 1.000 3 2008 2010