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: C4022863
Disease: Abnormal alpha granule content
Abnormal alpha granule content
phenotype Anatomical Abnormality 1 0.100 None 0
CUI: C1963099
Disease: Myelodysplasia, CTCAE
Myelodysplasia, CTCAE
phenotype Finding 68 0.100 None 0
CUI: C0015967
Disease: Fever
Fever
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 1021 66 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: C0015672
Disease: Fatigue
Fatigue
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 760 67 0.100 None 0 1
CUI: C0014591
Disease: Epistaxis
Epistaxis
phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Pathologic Function 82 4 0.100 None 0
CUI: C1334068
Disease: Hypercellular bone marrow
Hypercellular bone marrow
phenotype Finding 1 1 0.100 None 0 1
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
phenotype Pathological Conditions, Signs and Symptoms Finding 345 19 0.100 None 0
CUI: C0855997
Disease: Abnormal basophil morphology
Abnormal basophil morphology
phenotype Finding 3 0.100 None 0
CUI: C1855853
Disease: Impaired platelet aggregation
Impaired platelet aggregation
phenotype Finding 16 0.100 None 0
CUI: C0836924
Disease: Thrombocytosis
Thrombocytosis
disease Hemic and Lymphatic Diseases Disease or Syndrome 93 12 0.100 None 0
CUI: C0151529
Disease: Prolonged bleeding time
Prolonged bleeding time
phenotype Finding 39 3 0.100 None 0
CUI: C0232462
Disease: Decrease in appetite
Decrease in appetite
phenotype Digestive System Diseases; Nervous System Diseases; Mental Disorders Sign or Symptom 62 7 0.100 None 0
CUI: C0544886
Disease: Somatic mutation
Somatic mutation
phenotype Cell or Molecular Dysfunction 151 0.100 None 0
CUI: C0423798
Disease: Increased tendency to bruise
Increased tendency to bruise
phenotype Wounds and Injuries Finding 133 14 0.100 None 0
Therapy-related acute myeloid leukemia and myelodysplastic syndrome
disease Neoplasms Neoplastic Process 11 0.010 None 1.000 1 1993 1993
CUI: C2242826
Disease: Myeloblastic leukemia
Myeloblastic leukemia
disease Neoplastic Process 22 0.010 None 1.000 1 1994 1994
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: C0029925
Disease: Ovarian Carcinoma
Ovarian Carcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 539 19 0.010 None 1.000 1 1996 1996
Acute lymphoblastic leukemia, in relapse
disease Neoplastic Process 2 0.010 None 1.000 1 1997 1997
CUI: C0278721
Disease: Adult Lymphoblastic Lymphoma
Adult Lymphoblastic Lymphoma
disease Neoplastic Process 85 4 0.010 None 1.000 1 1998 1998
CUI: C0279525
Disease: Childhood Lymphoblastic Lymphoma
Childhood Lymphoblastic Lymphoma
disease Neoplastic Process 85 4 0.010 None 1.000 1 1998 1998
Precursor cell lymphoblastic lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 88 4 0.010 None 1.000 1 1998 1998
Refractory anemia with excess blasts in transformation (clinical)
disease Hemic and Lymphatic Diseases Disease or Syndrome 10 0.010 None 1.000 1 1999 1999
CUI: C0280745
Disease: secondary myelodysplastic syndromes
secondary myelodysplastic syndromes
disease Hemic and Lymphatic Diseases Neoplastic Process 11 0.020 None 1.000 2 1998 2000