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.
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6
disease Finding 1 1 0.300 None 1.000 1 1 2005 2005
Staphylococcus epidermidis infection
disease Infections Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C1956413
Disease: Taussig-Bing Anomaly
Taussig-Bing Anomaly
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 4 0.100 None 0
Decreased level of 1,5 anhydroglucitol in serum
phenotype Finding 4 0.100 None 0
CUI: C0221262
Disease: Poliosis
Poliosis
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 5 1 0.100 None 0
CUI: C0409983
Disease: Secondary antiphospholipid syndrome
Secondary antiphospholipid syndrome
disease Immune System Diseases Disease or Syndrome 6 0.010 None 1.000 1 2014 2014
CUI: C1387164
Disease: allergic rhinitis with asthma
allergic rhinitis with asthma
disease Disease or Syndrome 6 6 0.010 None 1.000 1 2016 2016
CUI: C1956391
Disease: Temporal Arteritis
Temporal Arteritis
disease Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 6 6 0.300 None 1.000 1 2013 2013
CUI: C2887821
Disease: Left sided colitis
Left sided colitis
disease Digestive System Diseases Disease or Syndrome 6 1 0.010 None 1.000 1 2013 2013
CUI: C0017675
Disease: Glossitis
Glossitis
disease Stomatognathic Diseases Disease or Syndrome 7 0.100 None 0
CUI: C3805919
Disease: Recurrent intrapulmonary hemorrhage
Recurrent intrapulmonary hemorrhage
phenotype Finding 7 0.100 None 0
CUI: C0747556
Disease: Recurrent pharyngitis
Recurrent pharyngitis
phenotype Infections; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Sign or Symptom 8 0.100 None 0
Polyglandular Type III Autoimmune Syndrome
disease Immune System Diseases; Endocrine System Diseases Disease or Syndrome 10 0.010 None 1.000 1 2015 2015
CUI: C0521618
Disease: Stenosis of ureter
Stenosis of ureter
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Anatomical Abnormality 10 0.100 None 0
CUI: C3152231
Disease: Gastrointestinal infarctions
Gastrointestinal infarctions
phenotype Finding 10 0.100 None 0
CUI: C4025726
Disease: Abnormality of the pleura
Abnormality of the pleura
disease Anatomical Abnormality 10 0.100 None 0
CUI: C0151854
Disease: Abnormal platelets
Abnormal platelets
phenotype Hemic and Lymphatic Diseases Cell or Molecular Dysfunction 11 0.100 None 0
CUI: C0036416
Disease: Scleritis
Scleritis
disease Eye Diseases Disease or Syndrome 12 0.010 None 1.000 1 2019 2019
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism
disease Endocrine System Diseases Disease or Syndrome 12 5 0.010 None 1.000 1 1 2006 2006
CUI: C3887590
Disease: Stricture of ureter
Stricture of ureter
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Anatomical Abnormality 12 0.100 None 0
CUI: C4025887
Disease: Abnormal oral cavity morphology
Abnormal oral cavity morphology
disease Anatomical Abnormality 12 0.100 None 0
CUI: C1692871
Disease: Inflammatory polyarthritis
Inflammatory polyarthritis
disease Disease or Syndrome 13 1 0.020 None 1.000 2 2008 2008
CUI: C0393847
Disease: Multifocal motor neuropathy
Multifocal motor neuropathy
disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 13 0.010 None < 0.001 1 2011 2011
CUI: C0277942
Disease: Butterfly rash
Butterfly rash
phenotype Skin and Connective Tissue Diseases Finding 13 0.100 None 0
CUI: C0085574
Disease: Palindromic rheumatism
Palindromic rheumatism
disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 14 2 0.010 None 1.000 1 2010 2010