IL17F, interleukin 17F, 112744

N. diseases: 236; 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.
CUI: C3151405
Disease: CANDIDIASIS, FAMILIAL, 6
CANDIDIASIS, FAMILIAL, 6
disease Disease or Syndrome 1 1 0.700 moderate 1.000 1 1 2011 2011
CUI: C0013289
Disease: Duodenal Diseases
Duodenal Diseases
group Digestive System Diseases Disease or Syndrome 5 2 0.010 None 1.000 1 1 2012 2012
CUI: C3888317
Disease: Sialidosis, type 2
Sialidosis, type 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 5 2 0.010 None 1.000 1 1981 1981
CUI: C1387164
Disease: allergic rhinitis with asthma
allergic rhinitis with asthma
disease Disease or Syndrome 6 6 0.010 None 1.000 1 2012 2012
Dianzani autoimmune lymphoproliferative syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 7 0.010 None 1.000 1 2014 2014
CUI: C0017657
Disease: Glomerulitis (disorder)
Glomerulitis (disorder)
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 8 1 0.010 None 1.000 1 1 2019 2019
CUI: C1843112
Disease: Broad nail
Broad nail
phenotype Finding 9 0.100 None 0
CUI: C0012243
Disease: Digestive System Neoplasms
Digestive System Neoplasms
group Digestive System Diseases; Neoplasms Neoplastic Process 12 2 0.010 None 1.000 1 1 2019 2019
CUI: C1856023
Disease: Abnormal vagina morphology
Abnormal vagina morphology
phenotype Finding 12 0.100 None 0
CUI: C0006848
Disease: Mucocutaneous candidiasis
Mucocutaneous candidiasis
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 15 0.010 None 1.000 1 2010 2010
CUI: C0152066
Disease: Lobomycosis
Lobomycosis
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 16 0.010 None 1.000 1 2015 2015
CUI: C0007971
Disease: Cheilitis
Cheilitis
disease Stomatognathic Diseases Disease or Syndrome 17 9 0.100 None 0
CUI: C2076602
Disease: Influenza A (H3N2)
Influenza A (H3N2)
disease Disease or Syndrome 18 1 0.010 None 1.000 1 2019 2019
Autoimmune polyendocrinopathy syndrome, type 1
disease Immune System Diseases; Endocrine System Diseases Disease or Syndrome 18 1 0.010 None 1.000 1 2010 2010
CUI: C0586407
Disease: Skin symptom
Skin symptom
phenotype Sign or Symptom 19 0.010 None 1.000 1 2018 2018
Abnormality of temperature regulation
phenotype Finding 19 3 0.100 None 0
CUI: C1504532
Disease: Post transplant diabetes mellitus
Post transplant diabetes mellitus
disease Disease or Syndrome 21 11 0.010 None 1.000 1 2 2015 2015
CUI: C3853962
Disease: Enterovirus 71 infection
Enterovirus 71 infection
disease Infections Disease or Syndrome 21 2 0.010 None 1.000 1 2018 2018
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 22 0.010 None 1.000 1 2018 2018
CUI: C4021662
Disease: Abnormal endocardium morphology
Abnormal endocardium morphology
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Anatomical Abnormality 23 0.100 None 0
CUI: C3839753
Disease: Abnormality of nail of toe
Abnormality of nail of toe
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 26 0.100 None 0
CUI: C0006845
Disease: Candidiasis, Chronic Mucocutaneous
Candidiasis, Chronic Mucocutaneous
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 31 3 0.450 None 1.000 6 2010 2018
CUI: C0041316
Disease: Lymph Node Tuberculosis
Lymph Node Tuberculosis
disease Infections Disease or Syndrome 33 1 0.020 None 1.000 2 2019 2019
CUI: C1384606
Disease: Dyspareunia
Dyspareunia
phenotype Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Mental Disorders Finding 37 0.100 None 0
CUI: C0340803
Disease: Capillary malformation (disorder)
Capillary malformation (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 40 13 0.030 None 1.000 3 2013 2017