TRNT1, tRNA nucleotidyl transferase 1, 51095

N. diseases: 40; N. variants: 15
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.
SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY
disease Disease or Syndrome 2 8 0.730 None 1.000 3 8 2014 2016
CUI: C0438434
Disease: Scotoma, Ring
Scotoma, Ring
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Sign or Symptom 2 0.100 None 0
RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS
disease Disease or Syndrome 2 3 0.600 strong 0 3
CUI: C0235988
Disease: Serum iron low (finding)
Serum iron low (finding)
phenotype Nutritional and Metabolic Diseases Finding 3 0.100 None 0
Photoreceptor layer loss on macular OCT
phenotype Finding 3 0.100 None 0
CUI: C0002891
Disease: Anemia, Neonatal
Anemia, Neonatal
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
CUI: C0855790
Disease: Decreased mean corpuscular volume
Decreased mean corpuscular volume
phenotype Finding 6 0.100 None 0
CUI: C0221018
Disease: Hereditary sideroblastic anemia
Hereditary sideroblastic anemia
disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 9 1 0.030 None 1.000 3 2014 2018
CUI: C0427480
Disease: Elliptocytosis found
Elliptocytosis found
phenotype Finding 12 0.100 None 0
CUI: C2698117
Disease: Anisocyte Measurement
Anisocyte Measurement
phenotype Laboratory Procedure 15 0.100 None 0
CUI: C0302254
Disease: Juvenile cataract
Juvenile cataract
disease Eye Diseases Anatomical Abnormality 16 3 0.010 None 1.000 1 2016 2016
CUI: C0221278
Disease: Anisocytosis
Anisocytosis
phenotype Finding 16 1 0.100 None 0
CUI: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 22 11 0.430 strong 1.000 3 2016 2019
CUI: C0013902
Disease: Elliptocytosis, Hereditary
Elliptocytosis, Hereditary
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 23 1 0.100 None 0
Microcytic hypochromic anemia (disorder)
disease Hemic and Lymphatic Diseases Disease or Syndrome 25 3 0.100 None 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy
phenotype Finding 25 4 0.100 None 0
CUI: C0522274
Disease: Humoral immune defect
Humoral immune defect
group Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 29 0.010 None 1.000 1 2019 2019
Iron-Refractory Iron Deficiency Anemia
disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 51 36 0.010 None 1.000 1 2019 2019
Extramedullary Hematopoiesis (disorder)
disease Hemic and Lymphatic Diseases Disease or Syndrome 52 1 0.010 None 1.000 1 2018 2018
CUI: C4048270
Disease: Decreased antibody level in blood
Decreased antibody level in blood
phenotype Finding 75 5 0.100 None 0
CUI: C0836924
Disease: Thrombocytosis
Thrombocytosis
disease Hemic and Lymphatic Diseases Disease or Syndrome 93 12 0.010 None 1.000 1 2019 2019
CUI: C0026946
Disease: Mycoses
Mycoses
group Infections Disease or Syndrome 94 2 0.010 None 1.000 1 2016 2016
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc
phenotype Finding 98 4 0.100 None 0
CUI: C0339543
Disease: Epiretinal Membrane
Epiretinal Membrane
disease Eye Diseases Acquired Abnormality 102 0.100 None 0
CUI: C0030232
Disease: Pallor
Pallor
phenotype Pathological Conditions, Signs and Symptoms Finding 124 4 0.100 None 0