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: C1849193
Disease: PEELING SKIN SYNDROME
PEELING SKIN SYNDROME
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 30 6 0.610 strong 1.000 6 4 1987 2014
CUI: C1840299
Disease: Hypotrichosis Simplex of Scalp
Hypotrichosis Simplex of Scalp
disease Skin and Connective Tissue Diseases Disease or Syndrome 3 2 0.600 3 2 1987 2003
CUI: C0018213
Disease: Graves Disease
Graves Disease
disease Endocrine System Diseases; Eye Diseases; Immune System Diseases Disease or Syndrome 334 213 0.110 1.000 2 2 1989 2012
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 1105 745 0.110 1.000 2 1 1989 2007
CUI: C0004096
Disease: Asthma
Asthma
disease Immune System Diseases; Respiratory Tract Diseases Disease or Syndrome 1312 729 0.110 1.000 2 1 2006 2017
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
disease Immune System Diseases; Musculoskeletal Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 1832 1878 0.110 1.000 2 1 2002 2009
CUI: C0033774
Disease: Pruritus
Pruritus
phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Finding 136 5 0.110 1.000 1 2010 2010
CUI: C1175175
Disease: Severe Acute Respiratory Syndrome
Severe Acute Respiratory Syndrome
disease Respiratory Tract Diseases; Virus Diseases Disease or Syndrome 84 1 0.100 1.000 21 2004 2016
CUI: C0033860
Disease: Psoriasis
Psoriasis
disease Skin and Connective Tissue Diseases Disease or Syndrome 817 636 0.100 0.923 13 1999 2016
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection
disease Disease or Syndrome 82 417 0.100 2 32 2010 2010
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
phenotype Laboratory Procedure 106 208 0.100 1 1 2010 2010
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
disease Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases Disease or Syndrome 257 225 0.100 1 2 2013 2013
CUI: C1851868
Disease: Reduced tensile strength of hair
Reduced tensile strength of hair
phenotype Finding 35 0.100 0
CUI: C0041834
Disease: Erythema
Erythema
phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 112 2 0.100 0
CUI: C1873509
Disease: Hypotrichosis of the scalp
Hypotrichosis of the scalp
phenotype Finding 10 0.100 0
CUI: C0236175
Disease: Increased IgE level
Increased IgE level
phenotype Finding 11 2 0.100 0
CUI: C1970705
Disease: Fragile hair
Fragile hair
phenotype Finding 35 0.100 0
CUI: C0349588
Disease: Short stature
Short stature
phenotype Finding 749 36 0.100 0
Abnormality of metabolism/homeostasis
group Finding 154 4 0.100 0
CUI: C3714497
Disease: Reactive airway disease
Reactive airway disease
disease Disease or Syndrome 27 0.100 0
CUI: C0085661
Disease: Onycholysis
Onycholysis
disease Skin and Connective Tissue Diseases Disease or Syndrome 9 0.100 0
CUI: C0263490
Disease: Brittle hair
Brittle hair
disease Disease or Syndrome 36 0.100 0
CUI: C0237849
Disease: Peeling of skin
Peeling of skin
phenotype Finding 11 0.100 0
CUI: C4072837
Disease: Fractured hair
Fractured hair
phenotype Finding 35 0.100 0
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
disease Digestive System Diseases; Virus Diseases Disease or Syndrome 838 192 0.060 1.000 6 1992 2013