ITGB2, integrin subunit beta 2, 3689

N. diseases: 340; N. variants: 31
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: C0423772
Disease: Cutaneous Fistula
Cutaneous Fistula 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Anatomical Abnormality 1 0.010 None 1.000 1 2017 2017
CUI: C4025198
Disease: Recurrent gram-negative bacterial infections
Recurrent gram-negative bacterial infections 		phenotype Finding 1 0.100 None 0
CUI: C0023510
Disease: Leukocyte Disorders
Leukocyte Disorders 		group Hemic and Lymphatic Diseases Disease or Syndrome 2 0.300 None 1.000 2 1987 1998
CUI: C4024862
Disease: Recurrent staphylococcal infections
Recurrent staphylococcal infections 		phenotype Finding 2 0.100 None 0
CUI: C0340319
Disease: Posterior myocardial infarction
Posterior myocardial infarction 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 3 0.010 None < 0.001 1 2017 2017
CUI: C4087338
Disease: Mite allergy
Mite allergy 		disease Disease or Syndrome 3 1 0.010 None 1.000 1 2001 2001
CUI: C0264695
Disease: Subendocardial ischemia
Subendocardial ischemia 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C1845609
Disease: Lymphoid depletion
Lymphoid depletion 		disease Disease or Syndrome 4 0.010 None 1.000 1 2001 2001
CUI: C0497299
Disease: meningitis/encephalitis
meningitis/encephalitis 		disease Disease or Syndrome 5 0.010 None 1.000 1 2001 2001
CUI: C2676767
Disease: CD59 Deficiency
CD59 Deficiency 		disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 5 4 0.010 None 1.000 1 2009 2009
CUI: C0242597
Disease: Leukocyte-Adhesion Deficiency Syndrome
Leukocyte-Adhesion Deficiency Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 6 0.300 None 1.000 1 1998 1998
CUI: C0262975
Disease: Chronic dermatitis
Chronic dermatitis 		disease Skin and Connective Tissue Diseases Disease or Syndrome 6 0.010 None 1.000 1 1998 1998
CUI: C0856737
Disease: Single vessel disease
Single vessel disease 		disease Cardiovascular Diseases Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
CUI: C2748536
Disease: Leukocyte Adhesion Deficiency, Type III
Leukocyte Adhesion Deficiency, Type III 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 7 6 0.020 None 0.500 2 2001 2010
CUI: C0398739
Disease: Congenital disorder of glycosylation, type 2C
Congenital disorder of glycosylation, type 2C 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 9 6 0.050 None 1.000 5 1998 2001
CUI: C0162442
Disease: Parapsoriasis en Plaques
Parapsoriasis en Plaques 		disease Skin and Connective Tissue Diseases Disease or Syndrome 9 0.010 None 1.000 1 2012 2012
CUI: C0240903
Disease: Rheumatoid Vasculitis
Rheumatoid Vasculitis 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 9 0.010 None 1.000 1 2001 2001
CUI: C0399451
Disease: Subgingival plaque
Subgingival plaque 		disease Stomatognathic Diseases Disease or Syndrome 9 0.010 None 1.000 1 2015 2015
CUI: C4285778
Disease: Systemic bacterial infection
Systemic bacterial infection 		disease Disease or Syndrome 9 0.010 None 1.000 1 2001 2001
CUI: C0149770
Disease: Rectal abscess
Rectal abscess 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Infections Pathologic Function 9 0.100 None 0
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: C2242472
Disease: Infection of bone
Infection of bone 		disease Pathological Conditions, Signs and Symptoms; Infections; Musculoskeletal Diseases Disease or Syndrome 11 0.010 None 1.000 1 1993 1993
CUI: C3536663
Disease: Acute deep venous thrombosis
Acute deep venous thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 11 0.010 None 1.000 1 2005 2005
CUI: C4743661
Disease: Leukocyte Adhesion Deficiency Type 3
Leukocyte Adhesion Deficiency Type 3 		disease Disease or Syndrome 11 3 0.010 None 1.000 1 2019 2019
CUI: C1264606
Disease: Persistent infection
Persistent infection 		phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 13 0.020 None 1.000 2 1999 2001