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: C1623038
Disease: Cirrhosis
Cirrhosis
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 815 110 0.040 None 0.750 4 1997 2018
Inherited predisposition to essential thrombocythemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 3 0.040 None 1.000 4 1998 2001
CUI: C0036690
Disease: Septicemia
Septicemia
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 1279 139 0.040 None 1.000 4 2010 2018
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1582 547 0.040 None 1.000 4 2001 2019
CUI: C0243026
Disease: Sepsis
Sepsis
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 1340 139 0.040 None 1.000 4 2010 2018
Thrombocytopenia-Absent Radius Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 9 1 0.030 None 1.000 3 1998 2012
CUI: C0349639
Disease: Juvenile Myelomonocytic Leukemia
Juvenile Myelomonocytic Leukemia
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 174 26 0.030 None 1.000 3 2015 2018
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: C0030312
Disease: Pancytopenia
Pancytopenia
disease Hemic and Lymphatic Diseases Disease or Syndrome 182 6 0.030 None 1.000 3 2017 2019
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
disease Neoplasms Neoplastic Process 1740 140 0.030 None 1.000 3 2016 2018
CUI: C0023418
Disease: leukemia
leukemia
disease Neoplasms Neoplastic Process 1984 138 0.030 None 1.000 3 2016 2018
CUI: C0023895
Disease: Liver diseases
Liver diseases
group Digestive System Diseases Disease or Syndrome 951 100 0.030 None 1.000 2 1998 2009
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.020 None 1.000 2 2015 2018
CUI: C0032463
Disease: Polycythemia Vera
Polycythemia Vera
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 283 37 0.020 None 1.000 2 2004 2016
Acquired amegakaryocytic thrombocytopenia
phenotype Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 2 0.020 None 1.000 2 2017 2019
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 5541 769 0.020 None 1.000 2 2000 2002
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 6500 2145 0.020 None 1.000 2 2018 2019
CUI: C4048329
Disease: Immunosuppression
Immunosuppression
disease Disease or Syndrome 632 9 0.020 None 1.000 2 2018 2019
CUI: C1883018
Disease: Severe Aplastic Anemia
Severe Aplastic Anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 69 4 0.020 None 1.000 2 2018 2018
CUI: C1854520
Disease: SEBASTIAN SYNDROME
SEBASTIAN SYNDROME
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 42 10 0.020 None 1.000 2 2011 2017
CUI: C0220621
Disease: Childhood Acute Myeloid Leukemia
Childhood Acute Myeloid Leukemia
disease Neoplasms Neoplastic Process 215 6 0.020 None 1.000 2 1998 2015
CUI: C1839163
Disease: THROMBOCYTOPENIA 1 (disorder)
THROMBOCYTOPENIA 1 (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 30 5 0.020 None 1.000 2 1996 1999
CUI: C0740404
Disease: Limb defects
Limb defects
group Congenital Abnormality 67 2 0.020 None 1.000 2 2009 2012
CUI: C0280962
Disease: Bone Marrow Suppression
Bone Marrow Suppression
disease Hemic and Lymphatic Diseases Disease or Syndrome 19 2 0.020 None 1.000 2 1996 2020
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