DEFB4A, defensin beta 4A, 1673

N. diseases: 177; N. variants: 0
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: C0040252
Disease: Tinea corporis (disorder)
Tinea corporis (disorder)
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 3 0.010 None 1.000 1 2007 2007
CUI: C0343029
Disease: Tuberculid
Tuberculid
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 5 0.010 None 1.000 1 2016 2016
CUI: C1960274
Disease: Nongonococcal cervicitis
Nongonococcal cervicitis
disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 5 0.010 None 1.000 1 2013 2013
CUI: C0040253
Disease: Tinea of perianal region
Tinea of perianal region
disease Disease or Syndrome 6 0.010 None 1.000 1 2015 2015
CUI: C1384589
Disease: Tinea cruris
Tinea cruris
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 6 0.010 None 1.000 1 2015 2015
CUI: C0042929
Disease: Polyp of vocal cord
Polyp of vocal cord
disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Neoplastic Process 9 0.010 None 1.000 1 2017 2017
CUI: C0041309
Disease: Tuberculosis, Cutaneous
Tuberculosis, Cutaneous
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 10 0.010 None 1.000 1 2016 2016
CUI: C0041582
Disease: Ulcer
Ulcer
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 11 0.010 None 1.000 1 2005 2005
CUI: C2242472
Disease: Infection of bone
Infection of bone
disease Pathological Conditions, Signs and Symptoms; Infections; Musculoskeletal Diseases Disease or Syndrome 11 0.010 None 1.000 1 2008 2008
CUI: C0239295
Disease: Candidiasis of the esophagus
Candidiasis of the esophagus
disease Digestive System Diseases; Infections Disease or Syndrome 12 0.020 None 1.000 2 2009 2011
CUI: C0406486
Disease: Ocular Rosacea
Ocular Rosacea
disease Skin and Connective Tissue Diseases Disease or Syndrome 12 0.010 None 1.000 1 2019 2019
Headache associated with sexual activity
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 14 0.010 None 1.000 1 2016 2016
CUI: C0456065
Disease: Infant, Extremely Low Birth Weight
Infant, Extremely Low Birth Weight
phenotype Disease or Syndrome 15 1 0.010 None 1.000 1 2012 2012
CUI: C4023560
Disease: Generalized periodontitis
Generalized periodontitis
disease Stomatognathic Diseases Disease or Syndrome 15 5 0.010 None 1.000 1 2015 2015
CUI: C0404521
Disease: Infective vaginitis
Infective vaginitis
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Infections Disease or Syndrome 18 0.010 None 1.000 1 2003 2003
CUI: C0011636
Disease: Dermatophytosis
Dermatophytosis
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 19 3 0.010 None 1.000 1 2015 2015
CUI: C0031736
Disease: Polymorphous light eruption
Polymorphous light eruption
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 20 0.010 None 1.000 1 2018 2018
CUI: C0040247
Disease: Tinea
Tinea
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 21 3 0.010 None 1.000 1 2015 2015
CUI: C0751560
Disease: Malignant neoplasm tonsil
Malignant neoplasm tonsil
disease Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases Neoplastic Process 22 0.010 None 1.000 1 2004 2004
CUI: C0558355
Disease: Tonsillar Carcinoma
Tonsillar Carcinoma
disease Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases Neoplastic Process 23 0.010 None 1.000 1 2004 2004
CUI: C1112211
Disease: Hepatic Infection
Hepatic Infection
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Infections Disease or Syndrome 24 0.010 None 1.000 1 2008 2008
CUI: C0023522
Disease: Leukodystrophy, Metachromatic
Leukodystrophy, Metachromatic
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 27 158 0.010 None 1.000 1 1991 1991
CUI: C0919659
Disease: Oropharyngeal candidiasis
Oropharyngeal candidiasis
disease Infections Disease or Syndrome 27 3 0.010 None 1.000 1 2017 2017
Insulin-Like Growth Factor I Deficiency
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 28 3 0.010 None 1.000 1 2012 2012
CUI: C0155490
Disease: Middle Ear Cholesteatoma
Middle Ear Cholesteatoma
disease Skin and Connective Tissue Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 29 0.020 None 1.000 2 2003 2007