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: C0278776
Disease: recurrent childhood acute myeloid leukemia
recurrent childhood acute myeloid leukemia 		disease Neoplastic Process 1 0.010 None 1.000 1 2014 2014
CUI: C1334068
Disease: Hypercellular bone marrow
Hypercellular bone marrow 		phenotype Finding 1 1 0.100 None 0 1
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: C0154733
Disease: Multiple cranial nerve palsy
Multiple cranial nerve palsy 		disease Nervous System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C2854088
Disease: Acute lymphoblastic leukemia, in relapse
Acute lymphoblastic leukemia, in relapse 		disease Neoplastic Process 2 0.010 None 1.000 1 1997 1997
CUI: C0398627
Disease: Inherited platelet disorder
Inherited platelet disorder 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C4552215
Disease: Autoimmune lung disease
Autoimmune lung disease 		disease Disease or Syndrome 3 0.010 None 1.000 1 2012 2012
CUI: C0855997
Disease: Abnormal basophil morphology
Abnormal basophil morphology 		phenotype Finding 3 0.100 None 0
CUI: C1832388
Disease: Platelet Disorder, Familial, with Associated Myeloid Malignancy
Platelet Disorder, Familial, with Associated Myeloid Malignancy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Hemic and Lymphatic Diseases Disease or Syndrome 4 20 0.730 definitive 1.000 31 20 1998 2019
CUI: C0585216
Disease: Alpha-Thalassemia Myelodysplasia Syndrome
Alpha-Thalassemia Myelodysplasia Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Neoplastic Process 4 3 0.010 None 1.000 1 2005 2005
CUI: C1533174
Disease: Acute myeloid leukemia, inv(16)(p13q22)
Acute myeloid leukemia, inv(16)(p13q22) 		disease Neoplastic Process 4 0.010 None 1.000 1 2014 2014
CUI: C2854122
Disease: Acute myeloblastic leukemia with t(8;21)
Acute myeloblastic leukemia with t(8;21) 		disease Neoplastic Process 4 0.010 None 1.000 1 2008 2008
CUI: C4733329
Disease: familial acute myeloid leukemia
familial acute myeloid leukemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms Disease or Syndrome 4 0.010 None 1.000 1 2016 2016
CUI: C0795856
Disease: Trisomy 15
Trisomy 15 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 5 0.010 None 1.000 1 2011 2011
CUI: C1275661
Disease: Acute myeloid leukemia with recurrent genetic abnormality
Acute myeloid leukemia with recurrent genetic abnormality 		disease Neoplasms Neoplastic Process 5 0.010 None 1.000 1 2016 2016
CUI: C1292773
Disease: Acute myeloid leukemia with multilineage dysplasia
Acute myeloid leukemia with multilineage dysplasia 		disease Neoplasms Neoplastic Process 5 0.010 None 1.000 1 2012 2012
CUI: C4707057
Disease: Tetrasomy 21
Tetrasomy 21 		disease Disease or Syndrome 6 0.030 None 1.000 3 2000 2004
CUI: C0005806
Disease: Blood Group Incompatibility
Blood Group Incompatibility 		disease Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
CUI: C2861614
Disease: AML M5b
AML M5b 		disease Neoplastic Process 6 0.010 None 1.000 1 2007 2007
CUI: C0162679
Disease: Leukemic Infiltration
Leukemic Infiltration 		phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 7 0.010 None 1.000 1 1996 1996
CUI: C1327915
Disease: Congenital amegakaryocytic thrombocytopenia
Congenital amegakaryocytic thrombocytopenia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Congenital Abnormality 7 25 0.010 None 1.000 1 2013 2013
CUI: C4704767
Disease: Myelodysplastic Syndrome Acute Myeloid Leukemia
Myelodysplastic Syndrome Acute Myeloid Leukemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Neoplastic Process 8 0.020 None 1.000 2 2012 2018
CUI: C0019624
Disease: Histiocytosis, Non-Langerhans-Cell
Histiocytosis, Non-Langerhans-Cell 		disease Hemic and Lymphatic Diseases Disease or Syndrome 9 2 0.010 None 1.000 1 2019 2019
CUI: C1737261
Disease: Acute myeloid leukaemia progression
Acute myeloid leukaemia progression 		disease Neoplastic Process 9 0.010 None 1.000 1 2014 2014