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: C0836924
Disease: Thrombocytosis
Thrombocytosis
disease Hemic and Lymphatic Diseases Disease or Syndrome 52 3 0.500 0.828 32 1995 2016
CUI: C0040028
Disease: Thrombocythemia, Essential
Thrombocythemia, Essential
disease Hemic and Lymphatic Diseases Disease or Syndrome 144 18 0.400 0.842 19 1996 2016
CUI: C0033141
Disease: Cardiomyopathies, Primary
Cardiomyopathies, Primary
group Cardiovascular Diseases Disease or Syndrome 91 0.300 1 2006 2006
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
group Cardiovascular Diseases Disease or Syndrome 479 108 0.300 1 2006 2006
CUI: C0036529
Disease: Myocardial Diseases, Secondary
Myocardial Diseases, Secondary
group Cardiovascular Diseases Disease or Syndrome 88 0.300 1 2006 2006
CUI: C4303761
Disease: Familial thrombocytosis
Familial thrombocytosis
disease Disease or Syndrome 3 0.300 0
CUI: C3489628
Disease: Thrombocytosis, Autosomal Dominant
Thrombocytosis, Autosomal Dominant
disease Hemic and Lymphatic Diseases Disease or Syndrome 9 0.300 0
CUI: C0027022
Disease: Myeloproliferative disease
Myeloproliferative disease
group Hemic and Lymphatic Diseases Neoplastic Process 263 23 0.160 1.000 6 1996 2016
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system
phenotype Anatomical Abnormality 87 5 0.110 1.000 1 2008 2008
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
phenotype Hemic and Lymphatic Diseases Disease or Syndrome 340 34 0.100 0.964 33 1995 2016
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 506 827 0.100 14 1 1997 2015
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
disease Neoplasms Neoplastic Process 1702 215 0.100 0.923 13 1995 2012
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis
disease Hemic and Lymphatic Diseases Neoplastic Process 181 20 0.100 0.900 10 1997 2018
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
phenotype Laboratory Procedure 190 353 0.100 1 3 2017 2017
CUI: C0474566
Disease: Platelet hematocrit measurement
Platelet hematocrit measurement
phenotype Laboratory Procedure 154 258 0.100 1 3 2017 2017
CUI: C0033774
Disease: Pruritus
Pruritus
phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Finding 136 5 0.100 0
CUI: C0038990
Disease: Sweating
Sweating
phenotype Finding 96 0.100 0
CUI: C0857460
Disease: Increased number of platelets
Increased number of platelets
phenotype Finding 15 0.100 0
CUI: C0085096
Disease: Peripheral Vascular Diseases
Peripheral Vascular Diseases
group Cardiovascular Diseases Disease or Syndrome 77 3 0.100 0
CUI: C0750145
Disease: Occlusive vascular disease
Occlusive vascular disease
disease Disease or Syndrome 16 0.100 0
CUI: C0700590
Disease: Increased sweating
Increased sweating
phenotype Finding 96 0.100 0
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
phenotype Pathological Conditions, Signs and Symptoms Finding 246 3 0.100 0
CUI: C0151942
Disease: Arterial thrombosis
Arterial thrombosis
phenotype Pathologic Function 10 0.100 0
CUI: C0030554
Disease: Paresthesia
Paresthesia
phenotype Nervous System Diseases; Pathological Conditions, Signs and Symptoms Disease or Syndrome 47 2 0.100 0
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis
phenotype Cardiovascular Diseases Pathologic Function 89 218 0.100 0