SH2B3, SH2B adaptor protein 3, 10019

N. diseases: 212; N. variants: 21
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
Precursor Cell Lymphoblastic Leukemia Lymphoma 		0.530 CausalMutation disease CGI
CUI: C0040028
Disease: Thrombocythemia, Essential
Thrombocythemia, Essential 		0.520 Biomarker disease CTD_human
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.420 Biomarker disease HPO
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.420 CausalMutation disease CLINVAR
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME 		0.410 Biomarker group HPO
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME 		0.410 CausalMutation group CGI
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME 		0.410 GenomicAlterations group CGI
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis 		0.400 CausalMutation disease CLINVAR
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis 		0.400 Biomarker disease HPO
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis 		0.400 Biomarker disease CTD_human
CUI: C4551637
Disease: Erythrocytosis familial, 1
Erythrocytosis familial, 1 		0.400 GeneticVariation disease CLINVAR
CUI: C4551637
Disease: Erythrocytosis familial, 1
Erythrocytosis familial, 1 		0.400 CausalMutation disease CLINVAR
CUI: C4551637
Disease: Erythrocytosis familial, 1
Erythrocytosis familial, 1 		0.400 Biomarker disease CTD_human
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.340 CausalMutation group CLINVAR
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.340 Biomarker group HPO
CUI: C0032463
Disease: Polycythemia Vera
Polycythemia Vera 		0.320 CausalMutation disease CGI
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms 		0.310 CausalMutation group CGI
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.300 CausalMutation disease CGI
CUI: C3489628
Disease: Thrombocytosis, Autosomal Dominant
Thrombocytosis, Autosomal Dominant 		0.300 Biomarker disease CTD_human
CUI: C0027022
Disease: Myeloproliferative disease
Myeloproliferative disease 		0.200 Biomarker group HPO
CUI: C0027022
Disease: Myeloproliferative disease
Myeloproliferative disease 		0.200 CausalMutation group CLINVAR
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		0.100 CausalMutation phenotype CLINVAR
CUI: C0003862
Disease: Arthralgia
Arthralgia 		0.100 CausalMutation phenotype CLINVAR
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders 		0.100 CausalMutation group CLINVAR
CUI: C0007787
Disease: Transient Ischemic Attack
Transient Ischemic Attack 		0.100 Biomarker disease HPO