TFRC, transferrin receptor, 7037

N. diseases: 359; N. variants: 40
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: C0003756
Disease: Arenaviridae Infections
Arenaviridae Infections 		group Infections Disease or Syndrome 1 0.300 None 1.000 1 2007 2007
CUI: C3711388
Disease: African Hemochromatosis
African Hemochromatosis 		disease Respiratory Tract Diseases; Occupational Diseases Disease or Syndrome 1 0.010 None < 0.001 1 1994 1994
CUI: C4225219
Disease: IMMUNODEFICIENCY 46
IMMUNODEFICIENCY 46 		disease Disease or Syndrome 1 2 0.700 None 1.000 1 2 2016 2016
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 4 3 0.010 None 1.000 1 2002 2002
CUI: C3826102
Disease: Iron deficiency anemia in children
Iron deficiency anemia in children 		disease Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C1839167
Disease: Intermittent thrombocytopenia
Intermittent thrombocytopenia 		phenotype Hemic and Lymphatic Diseases Finding 4 1 0.100 None 0
CUI: C0020058
Disease: Howell-Jolly Bodies
Howell-Jolly Bodies 		disease Acquired Abnormality 5 0.010 None 1.000 1 2007 2007
CUI: C0162679
Disease: Leukemic Infiltration
Leukemic Infiltration 		phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 7 0.010 None 1.000 1 2017 2017
CUI: C3844293
Disease: Oval fat body
Oval fat body 		phenotype Anatomical Abnormality 7 0.010 None 1.000 1 2017 2017
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 8 2 0.010 None 1.000 1 2003 2003
CUI: C0041976
Disease: Urethritis
Urethritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 9 0.010 None 1.000 1 1998 1998
CUI: C1320638
Disease: Bone marrow myeloid dysplasia
Bone marrow myeloid dysplasia 		disease Hemic and Lymphatic Diseases Neoplastic Process 9 0.010 None 1.000 1 2014 2014
CUI: C3805143
Disease: Non-transfusion dependent thalassaemia
Non-transfusion dependent thalassaemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 9 0.010 None 1.000 1 2017 2017
CUI: C0010474
Disease: Curling Ulcer
Curling Ulcer 		disease Digestive System Diseases Disease or Syndrome 12 0.200 None 1.000 1 2009 2009
CUI: C0205671
Disease: Infections, Arenavirus
Infections, Arenavirus 		group Infections Disease or Syndrome 12 0.300 None 1.000 1 2007 2007
CUI: C0205882
Disease: Infections, Parvovirus
Infections, Parvovirus 		group Infections Disease or Syndrome 12 0.010 None 1.000 1 2013 2013
CUI: C3714509
Disease: Nutrition Disorders
Nutrition Disorders 		group Nutritional and Metabolic Diseases Disease or Syndrome 12 0.200 None 1.000 1 2008 2008
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		group Nutritional and Metabolic Diseases Disease or Syndrome 15 3 0.300 None 1.000 2 2006 2007
CUI: C1332051
Disease: AIDS-Related Non-Hodgkin Lymphoma
AIDS-Related Non-Hodgkin Lymphoma 		disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 15 0.010 None 1.000 1 2013 2013
CUI: C1846546
Disease: Recurrent sinopulmonary infections
Recurrent sinopulmonary infections 		phenotype Finding 16 0.100 None 0
CUI: C0079487
Disease: Helicobacter Infections
Helicobacter Infections 		group Infections Disease or Syndrome 18 0.300 None 1.000 2 2006 2006
CUI: C0085578
Disease: Thalassemia Minor
Thalassemia Minor 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 18 1 0.300 None 1.000 1 2006 2006
CUI: C0043528
Disease: Zoonoses
Zoonoses 		disease Infections; Animal Diseases Disease or Syndrome 19 0.010 None 1.000 1 2017 2017
CUI: C0280962
Disease: Bone Marrow Suppression
Bone Marrow Suppression 		disease Hemic and Lymphatic Diseases Disease or Syndrome 19 2 0.010 None 1.000 1 2016 2016
CUI: C3550973
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 19 28 0.010 None 1.000 1 2017 2017