Source: BEFREE ×
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: C0275804
Disease: Streptococcal tonsillitis
Streptococcal tonsillitis
disease Infections; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C0278722
Disease: DS Stage I Plasma Cell Myeloma
DS Stage I Plasma Cell Myeloma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 2 0.010 None 1.000 1 1999 1999
CUI: C1096691
Disease: BK virus infection
BK virus infection
disease Infections Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
Undifferentiated inflammatory arthritis
disease Musculoskeletal Diseases Disease or Syndrome 2 0.010 None 1.000 1 2008 2008
CUI: C2346458
Disease: ISS Stage I Plasma Cell Myeloma
ISS Stage I Plasma Cell Myeloma
disease Neoplastic Process 2 0.010 None 1.000 1 1999 1999
CUI: C0853111
Disease: Late onset hypogammaglobulinemia
Late onset hypogammaglobulinemia
disease Disease or Syndrome 3 0.010 None 1.000 1 1991 1991
Asthma, Nasal Polyps, And Aspirin Intolerance
disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Immune System Diseases; Chemically-Induced Disorders; Otorhinolaryngologic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2008 2008
CUI: C0027339
Disease: Nail Diseases
Nail Diseases
group Skin and Connective Tissue Diseases Disease or Syndrome 4 1 0.010 None 1.000 1 2015 2015
CUI: C0040412
Disease: Fissured tongue
Fissured tongue
disease Stomatognathic Diseases Disease or Syndrome 4 0.010 None 1.000 1 2013 2013
CUI: C1617072
Disease: Infection caused by Lassa virus
Infection caused by Lassa virus
disease Infections Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C2830327
Disease: Tendency to fall
Tendency to fall
phenotype Sign or Symptom 4 1 0.010 None 1.000 1 2007 2007
CUI: C0032026
Disease: Pityriasis Rosea
Pityriasis Rosea
disease Skin and Connective Tissue Diseases Disease or Syndrome 5 0.010 None 1.000 1 2006 2006
CUI: C3899844
Disease: C4 Deficiency
C4 Deficiency
disease Disease or Syndrome 5 0.010 None 1.000 1 1994 1994
CUI: C0022073
Disease: Iridocyclitis
Iridocyclitis
disease Eye Diseases Disease or Syndrome 6 0.010 None 1.000 1 1997 1997
CUI: C0011573
Disease: Endogenous depression
Endogenous depression
disease Mental Disorders Mental or Behavioral Dysfunction 7 0.010 None 1.000 1 1993 1993
CUI: C0406322
Disease: Psoriasis of nail
Psoriasis of nail
disease Skin and Connective Tissue Diseases Disease or Syndrome 7 0.010 None 1.000 1 2014 2014
CUI: C0240903
Disease: Rheumatoid Vasculitis
Rheumatoid Vasculitis
disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 9 0.010 None 1.000 1 2015 2015
CUI: C0263367
Disease: Köbner phenomenon
Köbner phenomenon
disease Disease or Syndrome 9 0.010 None 1.000 1 2006 2006
CUI: C0271583
Disease: ACTH Deficiency, Isolated
ACTH Deficiency, Isolated
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 9 1 0.010 None 1.000 1 2019 2019
CUI: C0343052
Disease: Guttate psoriasis
Guttate psoriasis
disease Skin and Connective Tissue Diseases Disease or Syndrome 10 1 0.030 None 1.000 3 2000 2005
CUI: C0017980
Disease: Glycosuria, Renal
Glycosuria, Renal
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 10 5 0.010 None 1.000 1 1984 1984
CUI: C0029077
Disease: Ophthalmia, Sympathetic
Ophthalmia, Sympathetic
disease Eye Diseases; Immune System Diseases Disease or Syndrome 11 1 0.010 None 1.000 1 2001 2001
CUI: C1112570
Disease: Paraneoplastic pemphigus
Paraneoplastic pemphigus
disease Neoplasms Neoplastic Process 12 0.010 None 1.000 1 2008 2008
CUI: C3805083
Disease: Portal fibrosis
Portal fibrosis
phenotype Digestive System Diseases Disease or Syndrome 12 0.010 None 1.000 1 2019 2019
CUI: C1304140
Disease: Familial psoriasis
Familial psoriasis
disease Skin and Connective Tissue Diseases Disease or Syndrome 13 4 0.020 None 0.500 2 1 2002 2011