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: C1737229
Disease: Pemphigus herpetiformis
Pemphigus herpetiformis 		disease Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C2931122
Disease: Keratosis palmoplantaris striata 1
Keratosis palmoplantaris striata 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 1 8 0.600 strong 1.000 1 8 2017 2017
CUI: C4755302
Disease: Focal palmoplantar keratoderma with joint keratoses
Focal palmoplantar keratoderma with joint keratoses 		disease Disease or Syndrome 1 0.300 None 1.000 1 2006 2006
CUI: C4755309
Disease: Diffuse palmoplantar keratoderma with painful fissures
Diffuse palmoplantar keratoderma with painful fissures 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 1 0.300 None 1.000 1 2005 2005
CUI: C4024861
Disease: Streaks of hyperkeratosis along each finger onto the palm
Streaks of hyperkeratosis along each finger onto the palm 		phenotype Finding 1 0.100 None 0
CUI: C0740281
Disease: Multiple allergies
Multiple allergies 		disease Disease or Syndrome 2 0.020 None 1.000 2 2015 2016
CUI: C4021575
Disease: Diffuse palmoplantar hyperkeratosis
Diffuse palmoplantar hyperkeratosis 		disease Disease or Syndrome 2 1 0.100 None 0 1
CUI: C3809719
Disease: Severe dermatitis, multiple allergies, metabolic wasting syndrome
Severe dermatitis, multiple allergies, metabolic wasting syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 4 2 0.800 None 1.000 11 2 2013 2020
CUI: C0406650
Disease: Linear IgA Bullous Dermatosis
Linear IgA Bullous Dermatosis 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 4 0.010 None 1.000 1 2010 2010
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: C0021100
Disease: Bullous impetigo
Bullous impetigo 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 5 0.020 None 1.000 2 2009 2020
CUI: C1542647
Disease: bullous staphylococcal impetigo
bullous staphylococcal impetigo 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 5 0.020 None 1.000 2 2009 2020
CUI: C0038165
Disease: Staphylococcal Scalded Skin Syndrome
Staphylococcal Scalded Skin Syndrome 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 7 0.040 None 1.000 4 2005 2012
CUI: C0582591
Disease: Processing speed
Processing speed 		phenotype Mental Process 7 15 0.100 None 1.000 1 1 2014 2014
CUI: C0019343
Disease: Pemphigoid Gestationis
Pemphigoid Gestationis 		phenotype Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases Disease or Syndrome 8 0.010 None 1.000 1 2018 2018
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
CUI: C0021099
Disease: Impetigo
Impetigo 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 9 0.010 None 1.000 1 2003 2003
CUI: C0038166
Disease: Staphylococcal Skin Infections
Staphylococcal Skin Infections 		group Infections; Skin and Connective Tissue Diseases Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C1843359
Disease: Orthokeratosis
Orthokeratosis 		phenotype Skin and Connective Tissue Diseases Finding 10 0.100 None 0
CUI: C0000887
Disease: Acantholysis
Acantholysis 		phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Pathologic Function 11 0.100 None 0
CUI: C1112570
Disease: Paraneoplastic pemphigus
Paraneoplastic pemphigus 		disease Neoplasms Neoplastic Process 12 0.010 None 1.000 1 2010 2010
CUI: C3279547
Disease: Hypergranulosis
Hypergranulosis 		phenotype Finding 16 0.100 None 0
CUI: C0266574
Disease: Ablepharon
Ablepharon 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 20 1 0.010 None 1.000 1 2018 2018
CUI: C0022579
Disease: Keratoderma
Keratoderma 		disease Skin and Connective Tissue Diseases Congenital Abnormality 24 2 0.030 None 1.000 3 2003 2007
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