TET2, tet methylcytosine dioxygenase 2, 54790

N. diseases: 362; N. variants: 47
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: C4023019
Disease: Single lineage myelodysplasia
Single lineage myelodysplasia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.100 None 0
CUI: C4023036
Disease: Abnormal albumin level
Abnormal albumin level 		phenotype Finding 1 0.100 None 0
CUI: C0853655
Disease: Abnormal mean corpuscular volume
Abnormal mean corpuscular volume 		phenotype Finding 2 0.100 None 0
CUI: C4023021
Disease: Multiple lineage myelodysplasia
Multiple lineage myelodysplasia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 2 0.100 None 0
CUI: C4023029
Disease: Abnormal number of granulocyte precursors
Abnormal number of granulocyte precursors 		phenotype Anatomical Abnormality 2 0.100 None 0
CUI: C4023030
Disease: Dysplastic granulopoesis
Dysplastic granulopoesis 		disease Disease or Syndrome 2 0.100 None 0
CUI: C1333043
Disease: Chronic Myelomonocytic Leukemia-1
Chronic Myelomonocytic Leukemia-1 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 3 0.010 None 1.000 1 2009 2009
CUI: C1334688
Disease: Megaloblastic erythroid hyperplasia
Megaloblastic erythroid hyperplasia 		phenotype Finding 3 0.100 None 0
CUI: C1301365
Disease: Systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease
Systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease 		disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 4 0.300 None 1.000 1 2015 2015
CUI: C4023351
Disease: Hyposegmentation of neutrophil nuclei
Hyposegmentation of neutrophil nuclei 		phenotype Cell or Molecular Dysfunction 4 1 0.100 None 0
CUI: C0751246
Disease: Illusions, Visual
Illusions, Visual 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 5 0.010 None 1.000 1 2017 2017
CUI: C1292773
Disease: Acute myeloid leukemia with multilineage dysplasia
Acute myeloid leukemia with multilineage dysplasia 		disease Neoplasms Neoplastic Process 5 0.300 None 1.000 1 2009 2009
CUI: C0239574
Disease: Low grade fever
Low grade fever 		phenotype Pathological Conditions, Signs and Symptoms Finding 5 1 0.100 None 0
CUI: C0016199
Disease: Flank Pain
Flank Pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 6 0.100 None 0
CUI: C4280733
Disease: Abnormal cardiac ventricular function
Abnormal cardiac ventricular function 		phenotype Finding 6 0.100 None 0
CUI: C0231779
Disease: Heel toe gait
Heel toe gait 		phenotype Sign or Symptom 7 0.010 None 1.000 1 2019 2019
CUI: C1336554
Disease: T-Cell and NK-Cell Neoplasm
T-Cell and NK-Cell Neoplasm 		disease Neoplastic Process 7 0.010 None 1.000 1 2020 2020
CUI: C4025187
Disease: Increased megakaryocyte count
Increased megakaryocyte count 		phenotype Finding 7 0.100 None 0
CUI: C4552670
Disease: Portal Vein Thrombosis, CTCAE
Portal Vein Thrombosis, CTCAE 		phenotype Finding 7 0.100 None 0
CUI: C1333046
Disease: Myeloproliferative Neoplasm, Unclassifiable
Myeloproliferative Neoplasm, Unclassifiable 		disease Neoplastic Process 8 3 0.020 None 1.000 2 2013 2018
CUI: C0406191
Disease: Pseudofolliculitis
Pseudofolliculitis 		disease Disease or Syndrome 8 1 0.010 None 1.000 1 2019 2019
CUI: C2826177
Disease: Acute myeloid leukemia with mutated NPM1
Acute myeloid leukemia with mutated NPM1 		disease Neoplasms Neoplastic Process 8 0.010 None 1.000 1 2019 2019
CUI: C4025811
Disease: Anemic pallor
Anemic pallor 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 8 0.100 None 0
CUI: C1737261
Disease: Acute myeloid leukaemia progression
Acute myeloid leukaemia progression 		disease Neoplastic Process 9 0.010 None 1.000 1 2014 2014
CUI: C3272525
Disease: Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma
Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma 		disease Neoplastic Process 9 2 0.010 None 1.000 1 2018 2018