ITGA2B, integrin subunit alpha 2b, 3674

N. diseases: 20; N. variants: 30
Source: CURATED ×
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: C1861195
Disease: Glanzmann Thrombasthenia, Autosomal Dominant
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 3 2 1998 2013
CUI: C0040015
Disease: Thrombasthenia
Thrombasthenia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 2 49 0.800 definitive 0.977 27 27 1982 2020
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 62 198 0.570 None 0.667 1 1997 2017
CUI: C4304021
Disease: Autosomal dominant macrothrombocytopenia
Autosomal dominant macrothrombocytopenia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 7 0.500 None 1.000 1 2000 2011
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		phenotype Hemic and Lymphatic Diseases Disease or Syndrome 29 45 0.450 None 1.000 1 1 1998 2019
CUI: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 0.420 None 1.000 0 2005 2009
CUI: C0751956
Disease: Acute Cerebrovascular Accidents
Acute Cerebrovascular Accidents 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 54 0.310 None 1.000 1 1998 2019
CUI: C3854603
Disease: FNAITP
FNAITP 		disease Disease or Syndrome 6 1 0.310 None 1.000 0 2008 2008
CUI: C4552091
Disease: Polyarthritis, Juvenile, Rheumatoid Factor Negative
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: C3714758
Disease: Juvenile psoriatic arthritis
Juvenile psoriatic arthritis 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 131 0.300 None 1.000 1 2009 2009
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 131 76 0.300 None 1.000 1 2009 2009
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 28 78 0.300 None 1.000 1 1998 1998
CUI: C0007274
Disease: Carotid Artery Thrombosis
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: 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
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: C0087031
Disease: Juvenile-Onset Still Disease
Juvenile-Onset Still Disease 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 135 41 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 774 0.300 None 1.000 1 2014 2014
CUI: C4704862
Disease: Polyarthritis, Juvenile, Rheumatoid Factor Positive
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
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