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.
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
disease Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 86 3 0.010 None 1.000 1 2019 2019
CUI: C0085278
Disease: Antiphospholipid Syndrome
Antiphospholipid Syndrome
disease Immune System Diseases Disease or Syndrome 99 17 0.010 None 1.000 1 2003 2003
CUI: C0003862
Disease: Arthralgia
Arthralgia
phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Sign or Symptom 248 27 0.100 None 0
CUI: C0003864
Disease: Arthritis
Arthritis
disease Musculoskeletal Diseases Disease or Syndrome 1072 69 0.010 None 1.000 1 1991 1991
CUI: C0543699
Disease: ASA intolerant asthma
ASA intolerant asthma
disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 9 0.010 None 1.000 1 2005 2005
Aspirin exacerbated respiratory disease
disease Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases; Immune System Diseases; Chemically-Induced Disorders; Otorhinolaryngologic Diseases Disease or Syndrome 94 32 0.030 None 1.000 3 3 2013 2014
Associated Pulmonary Arterial Hypertension
disease Respiratory Tract Diseases Disease or Syndrome 22 4 0.010 None 1.000 1 2019 2019
CUI: C0004096
Disease: Asthma
Asthma
disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 2096 1536 0.400 None 1.000 11 2 1993 2013
CUI: C0856716
Disease: Asthma aspirin-sensitive
Asthma aspirin-sensitive
disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 8 0.010 None 1.000 1 2014 2014
CUI: C1319853
Disease: Asthma, Aspirin-Induced
Asthma, Aspirin-Induced
disease Respiratory Tract Diseases; Immune System Diseases; Chemically-Induced Disorders Disease or Syndrome 25 6 0.420 None 1.000 3 1 1997 2013
CUI: C0264423
Disease: Asthma, Occupational
Asthma, Occupational
disease Respiratory Tract Diseases; Immune System Diseases; Occupational Diseases Disease or Syndrome 42 2 0.030 None 1.000 3 2006 2014
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 384 698 0.010 None 1.000 1 2005 2005
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
disease Mental Disorders Mental or Behavioral Dysfunction 1071 331 0.010 None 1.000 1 2020 2020
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
disease Mental Disorders Mental or Behavioral Dysfunction 1112 395 0.020 None 1.000 2 2019 2020
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
Autoimmune Chronic Hepatitis
disease Digestive System Diseases; Immune System Diseases Disease or Syndrome 213 23 0.050 None 1.000 5 1 1992 2018
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
group Immune System Diseases Disease or Syndrome 1758 428 0.090 None 1.000 9 1992 2020
CUI: C4721555
Disease: Autoimmune hepatitis
Autoimmune hepatitis
disease Digestive System Diseases Disease or Syndrome 190 22 0.050 None 1.000 5 1 1992 2018
CUI: C0400936
Disease: Autoimmune liver disease
Autoimmune liver disease
disease Digestive System Diseases; Immune System Diseases Disease or Syndrome 26 3 0.010 None 1.000 1 1995 1995
CUI: C0004368
Disease: Autoimmune state
Autoimmune state
phenotype Pathologic Function 70 0.100 None 0
CUI: C0178468
Disease: Autoimmune thyroid disease
Autoimmune thyroid disease
disease Immune System Diseases; Endocrine System Diseases Disease or Syndrome 107 15 0.010 None 1.000 1 2019 2019
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
Autoimmune thyroid disease (AITD)
disease Disease or Syndrome 133 54 0.030 None 1.000 3 1995 2019
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis
disease Immune System Diseases; Endocrine System Diseases Disease or Syndrome 161 76 0.010 None 1.000 1 2015 2015
CUI: C2931418
Disease: Bare lymphocyte syndrome 2
Bare lymphocyte syndrome 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases Disease or Syndrome 27 6 0.010 None 1.000 1 2006 2006
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases Disease or Syndrome 502 243 0.020 None 1.000 2 1992 1999
CUI: C0005138
Disease: Berylliosis
Berylliosis
disease Respiratory Tract Diseases; Occupational Diseases Injury or Poisoning 11 0.500 None 1.000 7 1993 2012