THPO, thrombopoietin, 7066

N. diseases: 148; N. variants: 7
Source: BEFREE ×
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: C0026985
Disease: Myelodysplasia
Myelodysplasia 		disease Congenital Abnormality 135 3 0.120 None 1.000 2 1998 2012
CUI: C0740404
Disease: Limb defects
Limb defects 		group Congenital Abnormality 67 2 0.020 None 1.000 2 2009 2012
CUI: C4048329
Disease: Immunosuppression
Immunosuppression 		disease Disease or Syndrome 632 9 0.020 None 1.000 2 2018 2019
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		disease Neoplastic Process 3669 502 0.020 None 1.000 2 2015 2018
CUI: C0220810
Disease: Congenital defects
Congenital defects 		group Congenital Abnormality 126 6 0.010 None 1.000 1 2002 2002
CUI: C0235604
Disease: Qualitative platelet deficiency
Qualitative platelet deficiency 		disease Disease or Syndrome 3 1 0.010 None 1.000 1 2017 2017
CUI: C0749393
Disease: Chronic thrombocytopenia
Chronic thrombocytopenia 		disease Disease or Syndrome 1 0.010 None 1.000 1 2004 2004
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction 		phenotype Disease or Syndrome 716 25 0.010 None 1.000 1 2018 2018
CUI: C0948968
Disease: Osteomyelofibrosis
Osteomyelofibrosis 		disease Neoplastic Process 2 0.010 None 1.000 1 1998 1998
CUI: C1264031
Disease: Alloimmune thrombocytopenia
Alloimmune thrombocytopenia 		disease Disease or Syndrome 2 1 0.010 None 1.000 1 2001 2001
CUI: C1608426
Disease: Compensated cirrhosis
Compensated cirrhosis 		disease Disease or Syndrome 23 2 0.010 None 1.000 1 1999 1999
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		disease Disease or Syndrome 1075 276 0.010 None 1.000 1 2005 2005
CUI: C1879691
Disease: Amegakaryocytosis
Amegakaryocytosis 		disease Disease or Syndrome 1 0.010 None 1.000 1 2020 2020
CUI: C3854222
Disease: Human immunodeficiency virus (HIV) II infection category B1
Human immunodeficiency virus (HIV) II infection category B1 		disease Disease or Syndrome 985 56 0.010 None 1.000 1 2007 2007
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system 		disease Anatomical Abnormality 120 5 0.110 None 1.000 1 2008 2008
CUI: C4476767
Disease: Diffuse alveolar hemorrhage
Diffuse alveolar hemorrhage 		disease Disease or Syndrome 8 0.010 None 1.000 1 2018 2018
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		disease Disease or Syndrome 10 9 0.010 None 1.000 1 2019 2019
CUI: C0344315
Disease: Depressed mood
Depressed mood 		phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1459 269 0.010 None 1.000 1 2010 2010
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		disease Cardiovascular Diseases Disease or Syndrome 1504 1022 0.030 None 0.667 3 2017 2019
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		group Cardiovascular Diseases Disease or Syndrome 1551 382 0.010 None 1.000 1 2008 2008
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		disease Cardiovascular Diseases Disease or Syndrome 1262 440 0.010 None 1.000 1 2017 2017
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		disease Cardiovascular Diseases Disease or Syndrome 1432 769 0.010 None 1.000 1 2017 2017
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 1091 73 0.020 None 1.000 2 2002 2012
CUI: C0796070
Disease: MICROPHTHALMIA, SYNDROMIC 7
MICROPHTHALMIA, SYNDROMIC 7 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases Disease or Syndrome; Congenital Abnormality 46 2 0.010 None 1.000 1 2004 2004
CUI: C1327915
Disease: Congenital amegakaryocytic thrombocytopenia
Congenital amegakaryocytic thrombocytopenia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Congenital Abnormality 7 4 0.090 None 1.000 9 2 2000 2018