DSG4, desmoglein 4, 147409

N. diseases: 40; N. variants: 10
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.
Noonan-Like Syndrome With Loose Anagen Hair
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 22 4 0.010 None 1.000 1 2013 2013
CUI: C1862862
Disease: Patchy alopecia
Patchy alopecia
phenotype Skin and Connective Tissue Diseases Finding 8 0.100 None 0
CUI: C0030807
Disease: Pemphigus
Pemphigus
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 67 3 0.020 None 1.000 2 2003 2004
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 115 39 0.010 None 1.000 1 2003 2003
CUI: C0334013
Disease: Phrynoderma
Phrynoderma
disease Skin and Connective Tissue Diseases Disease or Syndrome 19 3 0.100 None 0
POLYARTERITIS NODOSA, CHILDHOOD-ONSET
disease Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 63 12 0.010 None 1.000 1 2019 2019
CUI: C0033774
Disease: Pruritus
Pruritus
phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Finding 107 2 0.100 None 0
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
disease Mental Disorders Mental or Behavioral Dysfunction 2872 2897 0.100 None 0
CUI: C1832348
Disease: Slow-growing hair
Slow-growing hair
phenotype Finding 35 1 0.100 None 0
CUI: C4282407
Disease: Sparse and thin eyebrow
Sparse and thin eyebrow
phenotype Finding 68 8 0.100 None 0
CUI: C1862863
Disease: Sparse body hair
Sparse body hair
phenotype Finding 57 0.100 None 0
CUI: C1843300
Disease: Sparse eyelashes
Sparse eyelashes
phenotype Finding 60 4 0.100 None 0
Staphylococcal Scalded Skin Syndrome
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 7 0.010 None 1.000 1 2004 2004
CUI: C0333307
Disease: Superficial ulcer
Superficial ulcer
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 242 10 0.010 None 1.000 1 2006 2006
CUI: C1836672
Disease: Total Hypotrichosis, Mari type
Total Hypotrichosis, Mari type
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 27 4 0.060 None 0.833 6 1 2006 2015