ITGB3, integrin subunit beta 3, 3690

N. diseases: 260; N. variants: 44
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0040015
Disease: Thrombasthenia
Thrombasthenia 		1.000 CausalMutation disease CLINVAR
CUI: C0040015
Disease: Thrombasthenia
Thrombasthenia 		1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C0040015
Disease: Thrombasthenia
Thrombasthenia 		1.000 Biomarker disease MGD
CUI: C0040015
Disease: Thrombasthenia
Thrombasthenia 		1.000 GeneticVariation disease CLINVAR
CUI: C0040015
Disease: Thrombasthenia
Thrombasthenia 		1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C1861195
Disease: Glanzmann Thrombasthenia, Autosomal Dominant
Glanzmann Thrombasthenia, Autosomal Dominant 		0.900 Biomarker disease GENOMICS_ENGLAND
CUI: C1861195
Disease: Glanzmann Thrombasthenia, Autosomal Dominant
Glanzmann Thrombasthenia, Autosomal Dominant 		0.900 CausalMutation disease CLINVAR
CUI: C1861195
Disease: Glanzmann Thrombasthenia, Autosomal Dominant
Glanzmann Thrombasthenia, Autosomal Dominant 		0.900 Biomarker disease CTD_human
CUI: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		0.770 Biomarker disease GENOMICS_ENGLAND
CUI: C3853779
Disease: Neonatal Alloimmune Thrombocytopenia
Neonatal Alloimmune Thrombocytopenia 		0.770 Biomarker disease HPO
CUI: C3854603
Disease: FNAITP
FNAITP 		0.400 GeneticVariation disease CLINVAR
CUI: C0398648
Disease: Posttransfusion purpura
Posttransfusion purpura 		0.300 Biomarker phenotype GENOMICS_ENGLAND
CUI: C1832662
Disease: MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO 		0.300 Biomarker phenotype GENOMICS_ENGLAND
CUI: C2751260
Disease: Macrothrombocytopenia
Macrothrombocytopenia 		0.140 Biomarker disease HPO
CUI: C0038525
Disease: Subarachnoid Hemorrhage
Subarachnoid Hemorrhage 		0.120 Biomarker disease HPO
CUI: C0002871
Disease: Anemia
Anemia 		0.100 Biomarker disease HPO
CUI: C0007722
Disease: Cephalhematoma due to birth trauma
Cephalhematoma due to birth trauma 		0.100 Biomarker phenotype HPO
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		0.100 Biomarker disease HPO
CUI: C0013491
Disease: Ecchymosis
Ecchymosis 		0.100 Biomarker phenotype HPO
CUI: C0014591
Disease: Epistaxis
Epistaxis 		0.100 Biomarker phenotype HPO
CUI: C0017181
Disease: Gastrointestinal Hemorrhage
Gastrointestinal Hemorrhage 		0.100 Biomarker phenotype HPO
CUI: C0017565
Disease: Gingival Hemorrhage
Gingival Hemorrhage 		0.100 Biomarker phenotype HPO
CUI: C0018965
Disease: Hematuria
Hematuria 		0.100 Biomarker phenotype HPO
CUI: C0025222
Disease: Melena
Melena 		0.100 Biomarker phenotype HPO
CUI: C0025323
Disease: Menorrhagia
Menorrhagia 		0.100 Biomarker phenotype HPO