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: C3711382
Disease: Familial Acute Myeloid Leukemia with Mutated Cebpa
Familial Acute Myeloid Leukemia with Mutated Cebpa 		disease Neoplasms Neoplastic Process 1 0.020 None 1.000 2 2013 2014
CUI: C0238740
Disease: severe back pain
severe back pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 1 0.010 None 1.000 1 2017 2017
CUI: C4054752
Disease: Hypocellular Myelodysplastic Syndrome
Hypocellular Myelodysplastic Syndrome 		disease Hemic and Lymphatic Diseases Neoplastic Process 1 0.010 None 1.000 1 2014 2014
CUI: C3275959
Disease: LEUKEMIA, ACUTE MYELOID, SUSCEPTIBILITY TO
LEUKEMIA, ACUTE MYELOID, SUSCEPTIBILITY TO 		phenotype Finding 1 7 0.100 None 0 6
CUI: C3279664
Disease: Emberger Syndrome
Emberger Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 2 15 0.770 None 1.000 21 15 2010 2018
CUI: C0275706
Disease: Infection due to Mycobacterium kansasii
Infection due to Mycobacterium kansasii 		disease Infections Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0427544
Disease: Monocytopenia
Monocytopenia 		phenotype Finding 2 0.100 None 0
CUI: C0580316
Disease: Neutrophil count abnormal
Neutrophil count abnormal 		phenotype Finding 2 1 0.100 None 0
CUI: C1737260
Disease: Recurrent mycobacterium avium complex infections
Recurrent mycobacterium avium complex infections 		phenotype Finding 2 0.100 None 0
CUI: C4021098
Disease: Abnormal natural killer cell morphology
Abnormal natural killer cell morphology 		disease Anatomical Abnormality 2 1 0.100 None 0
CUI: C4707228
Disease: Inherited acute myeloid leukemia
Inherited acute myeloid leukemia 		disease Neoplasms Neoplastic Process 4 0.300 None 1.000 2 2011 2015
CUI: C0020241
Disease: Hydroa Vacciniforme
Hydroa Vacciniforme 		disease Skin and Connective Tissue Diseases Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C0553576
Disease: Systemic mycosis
Systemic mycosis 		disease Pathological Conditions, Signs and Symptoms; Infections; Skin and Connective Tissue Diseases Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
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 2020 2020
CUI: C1708397
Disease: Hydroa vacciniforme-like lymphoma
Hydroa vacciniforme-like lymphoma 		disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 5 0.010 None 1.000 1 2016 2016
CUI: C0746882
Disease: Chronic neutropenia
Chronic neutropenia 		disease Disease or Syndrome 6 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 2015 2015
CUI: C0024228
Disease: Lymphatic Diseases
Lymphatic Diseases 		group Hemic and Lymphatic Diseases Disease or Syndrome 8 0.010 None 1.000 1 2018 2018
CUI: C0032587
Disease: Polyradiculoneuropathy
Polyradiculoneuropathy 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 8 0.010 None 1.000 1 2018 2018
CUI: C0085700
Disease: Chondromalacia
Chondromalacia 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 8 0.300 None 1.000 1 2010 2010
CUI: C0279619
Disease: Adult Acute Erythroid Leukemia
Adult Acute Erythroid Leukemia 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 8 0.010 None 1.000 1 2017 2017
CUI: C1332937
Disease: Childhood Acute Erythroid Leukemia
Childhood Acute Erythroid Leukemia 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 8 0.010 None 1.000 1 2017 2017
CUI: C4049615
Disease: Megaureter
Megaureter 		disease Congenital Abnormality 8 0.010 None 1.000 1 2008 2008
CUI: C3280030
Disease: GATA2 Deficiency
GATA2 Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 9 18 0.800 definitive 1.000 34 18 1994 2019
CUI: C0238261
Disease: Lymphedema praecox
Lymphedema praecox 		disease Hemic and Lymphatic Diseases Disease or Syndrome 9 0.030 None 1.000 3 2011 2017