ITGA2B, integrin subunit alpha 2b, 3674

N. diseases: 215; N. variants: 36
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.
Glanzmann Thrombasthenia, Autosomal Dominant
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 2 5 0.900 strong 1.000 4 2 1998 2013
CUI: C0040015
Disease: Thrombasthenia
Thrombasthenia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 48 61 0.800 definitive 0.977 87 29 1982 2020
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1658 591 0.570 None 0.667 9 1997 2017
Autosomal dominant macrothrombocytopenia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 9 0.500 None 1.000 2 2000 2011
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
phenotype Hemic and Lymphatic Diseases Disease or Syndrome 592 110 0.450 None 1.000 7 1 1998 2019
Neonatal Alloimmune Thrombocytopenia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 29 1 0.420 None 1.000 2 1 2005 2009
CUI: C0751956
Disease: Acute Cerebrovascular Accidents
Acute Cerebrovascular Accidents
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 155 2 0.310 None 1.000 2 1998 2019
CUI: C3854603
Disease: FNAITP
FNAITP
disease Disease or Syndrome 12 2 0.310 None 1.000 1 2008 2008
CUI: C0087031
Disease: Juvenile-Onset Still Disease
Juvenile-Onset Still Disease
disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 171 41 0.300 None 1.000 1 2009 2009
CUI: C0007274
Disease: Carotid Artery Thrombosis
Carotid Artery Thrombosis
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 30 0.300 None 1.000 1 1992 1992
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 122 78 0.300 None 1.000 1 1998 1998
CUI: C3714758
Disease: Juvenile psoriatic arthritis
Juvenile psoriatic arthritis
disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 138 0.300 None 1.000 1 2009 2009
CUI: C0023893
Disease: Liver Cirrhosis, Experimental
Liver Cirrhosis, Experimental
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Experimental Model of Disease 870 0.300 None 1.000 1 2014 2014
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 450 128 0.300 None 1.000 1 2009 2009
CUI: C0750989
Disease: External Carotid Artery Thrombosis
External Carotid Artery Thrombosis
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.300 None 1.000 1 1992 1992
Polyarthritis, Juvenile, Rheumatoid Factor Positive
disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 131 0.300 None 1.000 1 2009 2009
Polyarthritis, Juvenile, Rheumatoid Factor Negative
disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 131 0.300 None 1.000 1 2009 2009
CUI: C0750988
Disease: Common Carotid Artery Thrombosis
Common Carotid Artery Thrombosis
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.300 None 1.000 1 1992 1992
CUI: C0750990
Disease: Internal Carotid Artery Thrombosis
Internal Carotid Artery Thrombosis
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.300 None 1.000 1 1992 1992
CUI: C3179396
Disease: Glanzmann Thrombasthenia, Type A
Glanzmann Thrombasthenia, Type A
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 2 0.300 None 0
CUI: C0376618
Disease: Endotoxemia
Endotoxemia
phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 401 5 0.210 None 1.000 2 2003 2005
CUI: C0035126
Disease: Reperfusion Injury
Reperfusion Injury
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Injury or Poisoning 300 0.200 None 1.000 1 2001 2001
CUI: C0477317
Disease: Other primary thrombocytopenia
Other primary thrombocytopenia
group Hemic and Lymphatic Diseases Disease or Syndrome 3 0.200 None 1.000 1 2000 2000
CUI: C2751260
Disease: Macrothrombocytopenia
Macrothrombocytopenia
disease Hemic and Lymphatic Diseases Disease or Syndrome 34 31 0.130 None 1.000 3 1 2011 2018
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
disease Neoplasms Neoplastic Process 3111 6892 0.110 None 1.000 2 1 2014 2017