RUNX1, RUNX family transcription factor 1, 861

N. diseases: 412; N. variants: 75
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: C1737261
Disease: Acute myeloid leukaemia progression
Acute myeloid leukaemia progression
disease Neoplastic Process 9 0.010 None 1.000 1 2014 2014
CUI: C1739135
Disease: Progression of prostate cancer
Progression of prostate cancer
disease Neoplastic Process 398 7 0.010 None 1.000 1 2015 2015
CUI: C1855496
Disease: Contiguous gene syndrome
Contiguous gene syndrome
disease Disease or Syndrome 52 0.010 None 1.000 1 2016 2016
CUI: C2242826
Disease: Myeloblastic leukemia
Myeloblastic leukemia
disease Neoplastic Process 22 0.010 None 1.000 1 1994 1994
CUI: C2363774
Disease: Neutrophilic asthma
Neutrophilic asthma
disease Disease or Syndrome 40 2 0.010 None 1.000 1 2017 2017
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement
phenotype Laboratory Procedure 82 123 0.100 None 1.000 1 1 2012 2012
CUI: C2826025
Disease: Mixed phenotype acute leukemia
Mixed phenotype acute leukemia
disease Neoplastic Process 37 0.010 None 1.000 1 2010 2010
Myeloid/Lymphoid Neoplasms with FGFR1 Rearrangement
disease Neoplastic Process 22 0.010 None 1.000 1 2007 2007
Acute lymphoblastic leukemia, in relapse
disease Neoplastic Process 2 0.010 None 1.000 1 1997 1997
Acute myeloblastic leukemia with t(8;21)
disease Neoplastic Process 4 0.010 None 1.000 1 2008 2008
CUI: C2861614
Disease: AML M5b
AML M5b
disease Neoplastic Process 6 0.010 None 1.000 1 2007 2007
CUI: C4054726
Disease: Infant Leukemia
Infant Leukemia
disease Neoplastic Process 27 0.010 None 1.000 1 2009 2009
CUI: C4552215
Disease: Autoimmune lung disease
Autoimmune lung disease
disease Disease or Syndrome 3 0.010 None 1.000 1 2012 2012
estrogen receptor-negative breast cancer
disease Neoplastic Process 356 40 0.010 None 1.000 1 2011 2011
CUI: C0151529
Disease: Prolonged bleeding time
Prolonged bleeding time
phenotype Finding 39 3 0.100 None 0
CUI: C0544886
Disease: Somatic mutation
Somatic mutation
phenotype Cell or Molecular Dysfunction 151 0.100 None 0
CUI: C0855997
Disease: Abnormal basophil morphology
Abnormal basophil morphology
phenotype Finding 3 0.100 None 0
CUI: C1334068
Disease: Hypercellular bone marrow
Hypercellular bone marrow
phenotype Finding 1 1 0.100 None 0 1
CUI: C1855853
Disease: Impaired platelet aggregation
Impaired platelet aggregation
phenotype Finding 16 0.100 None 0
CUI: C1963099
Disease: Myelodysplasia, CTCAE
Myelodysplasia, CTCAE
phenotype Finding 68 0.100 None 0
CUI: C4021839
Disease: Abnormal dense granule content
Abnormal dense granule content
phenotype Anatomical Abnormality 1 0.100 None 0
CUI: C4022863
Disease: Abnormal alpha granule content
Abnormal alpha granule content
phenotype Anatomical Abnormality 1 0.100 None 0
CUI: C0085281
Disease: Addictive Behavior
Addictive Behavior
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 332 56 0.020 None 1.000 2 2013 2016
CUI: C0037369
Disease: Smoking
Smoking
phenotype Behavior and Behavior Mechanisms Individual Behavior 391 765 0.100 None 1.000 1 1 2015 2015
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
phenotype Behavior and Behavior Mechanisms Individual Behavior 249 742 0.100 None 1.000 1 1 2015 2015