DSG1, desmoglein 1, 1828

N. diseases: 81; N. variants: 13
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: C0000887
Disease: Acantholysis
Acantholysis
phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Pathologic Function 11 0.100 None 0
CUI: C0262985
Disease: Psoriasiform eczema
Psoriasiform eczema
disease Skin and Connective Tissue Diseases Disease or Syndrome 62 0.100 None 0
CUI: C0456070
Disease: Growth delay
Growth delay
phenotype Pathologic Function 244 40 0.100 None 0
CUI: C0020678
Disease: Hypotrichosis
Hypotrichosis
disease Skin and Connective Tissue Diseases Disease or Syndrome 69 2 0.100 None 0
CUI: C0020488
Disease: Hypernatremia
Hypernatremia
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 59 3 0.100 None 0
CUI: C0853087
Disease: Nail abnormality
Nail abnormality
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 67 11 0.100 None 0
CUI: C3279547
Disease: Hypergranulosis
Hypergranulosis
phenotype Finding 16 0.100 None 0
CUI: C1843359
Disease: Orthokeratosis
Orthokeratosis
phenotype Skin and Connective Tissue Diseases Finding 10 0.100 None 0
CUI: C1853193
Disease: Recurrent skin infections
Recurrent skin infections
phenotype Infections; Skin and Connective Tissue Diseases Disease or Syndrome 95 2 0.100 None 0
CUI: C3806482
Disease: Recurrent respiratory infections
Recurrent respiratory infections
phenotype Infections; Respiratory Tract Diseases Finding 318 7 0.100 None 0
CUI: C0221270
Disease: Acanthosis
Acanthosis
phenotype Pathological Conditions, Signs and Symptoms Finding 37 0.100 None 0
CUI: C0149630
Disease: Bicuspid aortic valve
Bicuspid aortic valve
disease Cardiovascular Diseases Congenital Abnormality 154 23 0.100 None 0 1
Streaks of hyperkeratosis along each finger onto the palm
phenotype Finding 1 0.100 None 0
CUI: C4021575
Disease: Diffuse palmoplantar hyperkeratosis
Diffuse palmoplantar hyperkeratosis
disease Disease or Syndrome 2 1 0.100 None 0 1
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
Hereditary Diffuse Gastric Cancer
disease Digestive System Diseases; Neoplasms Neoplastic Process 312 119 0.010 None 1.000 1 1992 1992
CUI: C0263313
Disease: Pemphigus Foliaceus
Pemphigus Foliaceus
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 51 16 0.100 None 0.980 49 1994 2019
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 115 39 0.100 None 0.951 41 1994 2019
CUI: C0030807
Disease: Pemphigus
Pemphigus
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 67 3 0.100 None 1.000 16 1995 2019
CUI: C0263314
Disease: Pemphigus and fogo selvagem
Pemphigus and fogo selvagem
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 26 3 0.100 None 1.000 13 1995 2018
CUI: C0011436
Disease: Dentinogenesis Imperfecta
Dentinogenesis Imperfecta
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Congenital Abnormality 35 7 0.070 None 1.000 7 1995 2010
CUI: C0037274
Disease: Dermatologic disorders
Dermatologic disorders
group Skin and Connective Tissue Diseases Disease or Syndrome 617 21 0.100 None 1.000 14 1997 2017
CUI: C4707237
Disease: Striate palmoplantar keratoderma
Striate palmoplantar keratoderma
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 5 1 0.400 None 0.909 11 1999 2019
CUI: C0025202
Disease: melanoma
melanoma
disease Neoplasms Neoplastic Process 3087 515 0.010 None 1.000 1 2001 2001
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
group Immune System Diseases Disease or Syndrome 1758 428 0.040 None 0.750 4 2002 2019
CUI: C0406632
Disease: Autoimmune skin disease
Autoimmune skin disease
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 9 0.030 None 1.000 3 2002 2019