ITGB3, integrin subunit beta 3, 3690

N. diseases: 260; N. variants: 44
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: C0398648
Disease: Posttransfusion purpura
Posttransfusion purpura 		phenotype Immune System Diseases; Hemic and Lymphatic Diseases Pathologic Function 1 0.300 None 0
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 7 3 1999 2018
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 1.000 2 1992 1992
CUI: C0398356
Disease: Abdominal aortic atherosclerosis
Abdominal aortic atherosclerosis 		disease Disease or Syndrome 2 0.010 None 1.000 1 1999 1999
CUI: C4021767
Disease: Decreased platelet glycoprotein IIb-IIIa
Decreased platelet glycoprotein IIb-IIIa 		phenotype Finding 2 0.100 None 0
CUI: C4476985
Disease: Impaired clot retraction
Impaired clot retraction 		phenotype Finding 2 0.100 None 0
CUI: C0477317
Disease: Other primary thrombocytopenia
Other primary thrombocytopenia 		group Hemic and Lymphatic Diseases Disease or Syndrome 3 0.200 None 1.000 3 1999 2007
CUI: C1739105
Disease: Platelet anisocytosis
Platelet anisocytosis 		phenotype Pathologic Function 3 0.100 None 0
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: 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: 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: C0751711
Disease: Anterior Ischemic Optic Neuropathy
Anterior Ischemic Optic Neuropathy 		disease Eye Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2010 2010
CUI: C4022611
Disease: Prolonged bleeding following circumcision
Prolonged bleeding following circumcision 		phenotype Pathologic Function 5 0.100 None 0
CUI: C1868251
Disease: Neonatal alloimmune thrombocytopenia (NAIT)
Neonatal alloimmune thrombocytopenia (NAIT) 		disease Disease or Syndrome 6 0.020 None 1.000 2 1994 1997
CUI: C4023154
Disease: Impaired ristocetin-induced platelet aggregation
Impaired ristocetin-induced platelet aggregation 		phenotype Pathologic Function 6 1 0.100 None 0
CUI: C0577698
Disease: Exercise-induced angina
Exercise-induced angina 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Sign or Symptom 7 5 0.010 None 1.000 1 1 2007 2007
CUI: C0750145
Disease: Occlusive vascular disease
Occlusive vascular disease 		disease Disease or Syndrome 7 1 0.010 None 1.000 1 1999 1999
CUI: C0007722
Disease: Cephalhematoma due to birth trauma
Cephalhematoma due to birth trauma 		phenotype Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Wounds and Injuries Disease or Syndrome 7 0.100 None 0
CUI: C2237512
Disease: cephalohematoma
cephalohematoma 		phenotype Finding 7 0.100 None 0
CUI: C4304021
Disease: Autosomal dominant macrothrombocytopenia
Autosomal dominant macrothrombocytopenia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 9 0.510 None 1.000 6 1999 2018
CUI: C0473237
Disease: Frank hematuria
Frank hematuria 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 9 1 0.100 None 0
CUI: C1832662
Disease: MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO 		phenotype Finding 9 3 0.300 None 0
CUI: C1861185
Disease: THROMBOCYTOPENIA 2 (disorder)
THROMBOCYTOPENIA 2 (disorder) 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 10 4 0.010 None 1.000 1 1 2013 2013
CUI: C0232943
Disease: Intermenstrual heavy bleeding
Intermenstrual heavy bleeding 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Sign or Symptom 10 1 0.100 None 0
CUI: C0333864
Disease: Giant platelet (morphologic abnormality)
Giant platelet (morphologic abnormality) 		phenotype Finding 10 0.100 None 0