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: C4521042
Disease: Complete Trisomy 21 Syndrome
Complete Trisomy 21 Syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 669 77 0.010 None < 0.001 1 2012 2012
CUI: C0266999
Disease: Vesicular Stomatitis
Vesicular Stomatitis
disease Infections; Stomatognathic Diseases; Animal Diseases Disease or Syndrome 112 0.010 None 1.000 1 2010 2010
CUI: C0243026
Disease: Sepsis
Sepsis
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 1453 144 0.010 None 1.000 1 2018 2018
CUI: C0243010
Disease: Viral Encephalitis
Viral Encephalitis
group Infections; Nervous System Diseases Disease or Syndrome 35 0.010 None 1.000 1 2018 2018
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
Cervical Intraepithelial Neoplasia
disease Neoplasms Neoplastic Process 398 29 0.010 None 1.000 1 2009 2009
CUI: C0205734
Disease: Diabetes, Autoimmune
Diabetes, Autoimmune
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 172 4 0.010 None 1.000 1 2017 2017
CUI: C0151798
Disease: Hepatic necrosis
Hepatic necrosis
phenotype Digestive System Diseases Disease or Syndrome 44 0.010 None 1.000 1 2018 2018
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 403 96 0.010 None 1.000 1 2013 2013
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
disease Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 639 50 0.010 None 1.000 1 2018 2018
CUI: C0085110
Disease: Severe Combined Immunodeficiency
Severe Combined Immunodeficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases Disease or Syndrome 284 46 0.010 None 1.000 1 2004 2004
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
disease Infections Disease or Syndrome 1256 328 0.010 None 1.000 1 2014 2014
CUI: C0038826
Disease: Superinfection
Superinfection
group Infections Disease or Syndrome 85 0.010 None 1.000 1 2018 2018
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1658 591 0.010 None 1.000 1 2017 2017
CUI: C0037221
Disease: Situs Inversus
Situs Inversus
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 138 6 0.010 None 1.000 1 2018 2018
CUI: C0036690
Disease: Septicemia
Septicemia
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 1285 141 0.010 None 1.000 1 2018 2018
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
disease Skin and Connective Tissue Diseases Disease or Syndrome 979 287 0.010 None 1.000 1 1 2008 2008
Respiratory Syncytial Virus Infections
group Infections Disease or Syndrome 244 5 0.010 None 1.000 1 2017 2017
CUI: C0275524
Disease: Coinfection
Coinfection
phenotype Infections Disease or Syndrome 252 11 0.010 None 1.000 1 2001 2001
CUI: C0276609
Disease: Acute type B viral hepatitis
Acute type B viral hepatitis
disease Digestive System Diseases; Infections Disease or Syndrome 38 0.010 None 1.000 1 2016 2016
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma
disease Neoplasms Neoplastic Process 2420 231 0.010 None 1.000 1 1999 1999
CUI: C4048329
Disease: Immunosuppression
Immunosuppression
disease Disease or Syndrome 632 9 0.010 None 1.000 1 2010 2010
CUI: C3875321
Disease: Inflammatory dermatosis
Inflammatory dermatosis
disease Skin and Connective Tissue Diseases Disease or Syndrome 382 6 0.010 None 1.000 1 2016 2016
Disseminated Bacillus Calmette-Guerin infection
disease Infections Disease or Syndrome 5 0.010 None 1.000 1 1998 1998
CUI: C3714514
Disease: Infection
Infection
group Infections Pathologic Function 491 0.010 None 1.000 1 2006 2006
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 23 83 0.010 None 1.000 1 2016 2016