GATA2, GATA binding protein 2, 2624

N. diseases: 229; N. variants: 33
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: C0024116
Disease: Lung Diseases, Fungal
Lung Diseases, Fungal
group Infections; Respiratory Tract Diseases Disease or Syndrome 9 0.200 None 1.000 1 2006 2006
Core binding factor acute myeloid leukemia
disease Neoplasms Neoplastic Process 18 3 0.010 None 1.000 1 2020 2020
CUI: C0029131
Disease: Abnormality of the optic nerve
Abnormality of the optic nerve
phenotype Finding 18 11 0.100 None 0
CUI: C1844384
Disease: Recurrent fungal infections
Recurrent fungal infections
phenotype Finding 20 2 0.100 None 0
CUI: C0007302
Disease: Cartilage Diseases
Cartilage Diseases
group Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 23 0.300 None 1.000 1 2010 2010
CUI: C0740451
Disease: Granulomatous disorder
Granulomatous disorder
group Disease or Syndrome 26 1 0.010 None 1.000 1 2015 2015
CUI: C1837066
Disease: Recurrent viral infection
Recurrent viral infection
phenotype Infections Finding 32 0.100 None 0
Acute monocytic/monoblastic leukemia
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 35 2 0.010 None 1.000 1 2016 2016
CUI: C0206658
Disease: Smooth Muscle Tumor
Smooth Muscle Tumor
disease Neoplasms Neoplastic Process 36 0.020 None 1.000 2 2017 2018
CUI: C0876991
Disease: Histiocytosis haematophagic
Histiocytosis haematophagic
disease Disease or Syndrome 36 2 0.010 None 1.000 1 2017 2017
CUI: C2713368
Disease: Hematopoetic Myelodysplasia
Hematopoetic Myelodysplasia
phenotype Hemic and Lymphatic Diseases Pathologic Function 38 0.300 None 1.000 3 2011 2017
CUI: C0007642
Disease: Cellulitis
Cellulitis
phenotype Pathological Conditions, Signs and Symptoms; Infections; Skin and Connective Tissue Diseases Pathologic Function 38 1 0.100 None 0
CUI: C0151529
Disease: Prolonged bleeding time
Prolonged bleeding time
phenotype Finding 39 3 0.100 None 0
CUI: C0151699
Disease: Intracranial Hemorrhage
Intracranial Hemorrhage
group Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 40 2 0.100 None 0
CUI: C2931245
Disease: Bone Marrow failure syndromes
Bone Marrow failure syndromes
disease Disease or Syndrome 41 0.020 None 1.000 2 2014 2015
CUI: C0042063
Disease: Urogenital Abnormalities
Urogenital Abnormalities
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Congenital Abnormality 42 3 0.010 None 1.000 1 2008 2008
Therapy-related myelodysplastic syndrome
disease Hemic and Lymphatic Diseases Neoplastic Process 42 0.010 None 1.000 1 2016 2016
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1
disease Nervous System Diseases Disease or Syndrome 46 27 0.010 None 1.000 1 2008 2008
CUI: C1739405
Disease: CML progression
CML progression
disease Neoplastic Process 47 3 0.010 None 1.000 1 1 2009 2009
Refractory anaemia with excess blasts
disease Hemic and Lymphatic Diseases Neoplastic Process 49 2 0.020 None 1.000 2 2016 2019
acute myeloid leukemia with multilineage dysplasia following myelodysplastic syndrome
disease Neoplastic Process 49 1 0.010 None 1.000 1 2013 2013
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease
disease Nervous System Diseases Disease or Syndrome 51 32 0.010 None 1.000 1 2016 2016
CUI: C1704423
Disease: Milroy Disease
Milroy Disease
disease Hemic and Lymphatic Diseases Disease or Syndrome 52 18 0.340 None 1.000 4 2011 2017
CUI: C0278838
Disease: Prostate cancer recurrent
Prostate cancer recurrent
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 54 0.010 None < 0.001 1 2017 2017
Mycobacterium avium-intracellulare Infection
disease Infections Disease or Syndrome 58 5 0.010 None 1.000 1 2015 2015