THPO, thrombopoietin, 7066

N. diseases: 185; N. variants: 9
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: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
phenotype Laboratory Procedure 265 457 0.100 None 1.000 5 3 2010 2018
CUI: C0026985
Disease: Myelodysplasia
Myelodysplasia
disease Congenital Abnormality 181 4 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: C3277671
Disease: THROMBOCYTHEMIA 1
THROMBOCYTHEMIA 1
disease Disease or Syndrome 5 4 0.300 None 1.000 2 2012 2018
CUI: C4048329
Disease: Immunosuppression
Immunosuppression
disease Disease or Syndrome 632 9 0.020 None 1.000 2 2018 2019
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.020 None 1.000 2 2015 2018
Platelet mean volume determination (procedure)
phenotype Laboratory Procedure 223 371 0.100 None 1.000 1 1 2012 2012
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
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 148 18 0.110 None 1.000 1 2008 2008
CUI: C4476767
Disease: Diffuse alveolar hemorrhage
Diffuse alveolar hemorrhage
disease Disease or Syndrome 21 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: C0544886
Disease: Somatic mutation
Somatic mutation
phenotype Cell or Molecular Dysfunction 151 0.100 None 0
CUI: C1855853
Disease: Impaired platelet aggregation
Impaired platelet aggregation
phenotype Finding 16 0.100 None 0
CUI: C1963099
Disease: Myelodysplasia, CTCAE
Myelodysplasia, CTCAE
phenotype Finding 68 0.100 None 0
CUI: C4025272
Disease: Peripheral arterial stenosis
Peripheral arterial stenosis
disease Disease or Syndrome 124 5 0.100 None 0
CUI: C0344315
Disease: Depressed mood
Depressed mood
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1461 269 0.010 None 1.000 1 2010 2010