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: C2697501
Disease: Giant Platelet Count (procedure)
Giant Platelet Count (procedure) 		phenotype Laboratory Procedure 10 0.100 None 0
CUI: C0007772
Disease: Intracranial Arteriovenous Malformation
Intracranial Arteriovenous Malformation 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases Congenital Abnormality 11 0.010 None 1.000 1 2006 2006
CUI: C0242594
Disease: Residual Cancer
Residual Cancer 		phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 11 0.010 None 1.000 1 2017 2017
CUI: C3809715
Disease: Spontaneous, recurrent epistaxis
Spontaneous, recurrent epistaxis 		phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Sign or Symptom 11 1 0.100 None 0
CUI: C4021646
Disease: Prolonged bleeding after surgery
Prolonged bleeding after surgery 		phenotype Pathologic Function 11 0.100 None 0
CUI: C3854603
Disease: FNAITP
FNAITP 		disease Disease or Syndrome 12 2 0.400 None 1.000 1 1 2010 2010
CUI: C0265808
Disease: Cyanotic congenital heart disease
Cyanotic congenital heart disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 14 0.010 None 1.000 1 2001 2001
CUI: C0021308
Disease: Infarction
Infarction 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 15 0.010 None 1.000 1 2008 2008
CUI: C0025222
Disease: Melena
Melena 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Pathologic Function 15 1 0.100 None 0
CUI: C1855853
Disease: Impaired platelet aggregation
Impaired platelet aggregation 		phenotype Finding 16 0.100 None 0
CUI: C0333209
Disease: Platelet thrombus
Platelet thrombus 		disease Cardiovascular Diseases Acquired Abnormality 17 0.010 None 1.000 1 2001 2001
CUI: C0272278
Disease: Congenital thrombocytopenia
Congenital thrombocytopenia 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 19 3 0.010 None 1.000 1 2018 2018
CUI: C2584409
Disease: Prothrombin G20210A mutation
Prothrombin G20210A mutation 		disease Hemic and Lymphatic Diseases Disease or Syndrome 20 9 0.010 None 1.000 1 2004 2004
CUI: C0014084
Disease: Enchondromatosis
Enchondromatosis 		disease Musculoskeletal Diseases Disease or Syndrome 22 2 0.010 None 1.000 1 2019 2019
CUI: C0003499
Disease: Supravalvular aortic stenosis
Supravalvular aortic stenosis 		disease Cardiovascular Diseases Disease or Syndrome 23 38 0.010 None 1.000 1 2016 2016
CUI: C0013366
Disease: Dyschondroplasias
Dyschondroplasias 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 24 0.010 None 1.000 1 2019 2019
CUI: C0018915
Disease: Hemangioendothelioma
Hemangioendothelioma 		disease Neoplasms Neoplastic Process 26 0.010 None 1.000 1 2017 2017
CUI: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 29 1 0.770 None 1.000 10 1990 2019
CUI: C1334815
Disease: Multi-centric Castleman's Disease
Multi-centric Castleman's Disease 		disease Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 29 0.010 None 1.000 1 2020 2020
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: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas 		disease Disease or Syndrome 33 0.100 None 0
CUI: C2751260
Disease: Macrothrombocytopenia
Macrothrombocytopenia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 34 31 0.140 None 1.000 4 2008 2018
CUI: C0025323
Disease: Menorrhagia
Menorrhagia 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Pathologic Function 34 6 0.100 None 0
CUI: C0010072
Disease: Coronary Thrombosis
Coronary Thrombosis 		disease Cardiovascular Diseases Disease or Syndrome 35 2 0.350 None 1.000 6 1 1996 2014
CUI: C0003838
Disease: Arterial Occlusive Diseases
Arterial Occlusive Diseases 		group Cardiovascular Diseases Disease or Syndrome 35 4 0.200 None 1.000 1 1997 1997