EPO, erythropoietin, 2056

N. diseases: 646; N. variants: 11
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: C0549448
Disease: Hemoglobin increased
Hemoglobin increased
phenotype Neoplasms; Hemic and Lymphatic Diseases Finding 7 0.100 None 0
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 2 (finding)
disease Finding 1 1 0.300 None 0 1
CUI: C0239935
Disease: Hematocrit increased
Hematocrit increased
phenotype Finding 7 1 0.100 None 0
CUI: C0022665
Disease: Kidney Neoplasm
Kidney Neoplasm
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 295 11 0.010 None 1.000 1 1985 1985
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 0.020 None 1.000 2 1984 1986
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 852 704 0.020 None 1.000 2 1986 1987
Infant Acute Undifferentiated Leukemia
disease Neoplastic Process 14 0.010 None 1.000 1 1987 1987
CUI: C0280141
Disease: Acute Undifferentiated Leukemia
Acute Undifferentiated Leukemia
disease Neoplastic Process 119 1 0.010 None 1.000 1 1987 1987
CUI: C0005699
Disease: Blast Phase
Blast Phase
disease Pathological Conditions, Signs and Symptoms; Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 299 14 0.010 None 1.000 1 1987 1987
CUI: C0026499
Disease: Monosomy
Monosomy
group Pathological Conditions, Signs and Symptoms Congenital Abnormality 214 11 0.010 None 1.000 1 1987 1987
CUI: C1332900
Disease: Cerebellar hemangioblastoma
Cerebellar hemangioblastoma
disease Neoplasms; Nervous System Diseases Neoplastic Process 6 4 0.010 None 1.000 1 1991 1991
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 1172 115 0.030 None 1.000 3 1981 1993
CUI: C0025286
Disease: Meningioma
Meningioma
disease Neoplasms; Nervous System Diseases Neoplastic Process 634 43 0.010 None 1.000 1 1993 1993
CUI: C0751039
Disease: Cockayne Syndrome, Type I
Cockayne Syndrome, Type I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 80 42 0.010 None 1.000 1 1993 1993
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome
group Infections; Immune System Diseases Disease or Syndrome 243 42 0.010 None 1.000 1 1993 1993
CUI: C0278877
Disease: Adult Meningioma
Adult Meningioma
disease Neoplasms; Nervous System Diseases Neoplastic Process 405 30 0.010 None 1.000 1 1993 1993
CUI: C0599055
Disease: Waldenstrom's disease
Waldenstrom's disease
disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 2 1 0.010 None 1.000 1 1993 1993
CUI: C1262477
Disease: Weight decreased
Weight decreased
phenotype Pathological Conditions, Signs and Symptoms Finding 271 3 0.300 None 1.000 1 1993 1993
CUI: C0020455
Disease: Hypergammaglobulinemia
Hypergammaglobulinemia
disease Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 36 0.010 None 1.000 1 1993 1993
Meningioma, benign, no ICD-O subtype
disease Neoplasms; Nervous System Diseases Neoplastic Process 404 30 0.010 None 1.000 1 1993 1993
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 45 1 0.010 None 1.000 1 1995 1995
Myelodysplastic Syndrome with Isolated del(5q)
disease Hemic and Lymphatic Diseases Neoplastic Process 41 1 0.010 None 1.000 1 1995 1995
CUI: C1802398
Disease: Chromosome 5, trisomy 5q
Chromosome 5, trisomy 5q
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 42 1 0.010 None 1.000 1 1995 1995
CUI: C0020258
Disease: Hydrocephalus, Normal Pressure
Hydrocephalus, Normal Pressure
disease Nervous System Diseases Disease or Syndrome 44 6 0.010 None 1.000 1 1996 1996
CUI: C1883018
Disease: Severe Aplastic Anemia
Severe Aplastic Anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 70 4 0.010 None 1.000 1 1996 1996