FAS, Fas cell surface death receptor, 355

N. diseases: 66; N. variants: 38
Source: CURATED ×
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.
Autoimmune Lymphoproliferative Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 8 10 1.000 strong 1.000 18 10 1978 2018
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
group Immune System Diseases Disease or Syndrome 42 231 0.400 None 0.974 3 1989 2020
CUI: C0033141
Disease: Cardiomyopathies, Primary
Cardiomyopathies, Primary
group Cardiovascular Diseases Disease or Syndrome 69 1 0.300 None 1.000 3 2000 2007
CUI: C0036529
Disease: Myocardial Diseases, Secondary
Myocardial Diseases, Secondary
group Cardiovascular Diseases Disease or Syndrome 69 0.300 None 1.000 3 2000 2007
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
group Cardiovascular Diseases Disease or Syndrome 130 172 0.300 None 1.000 3 2000 2007
Autoimmune Lymphoproliferative Syndrome Type 2B
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 7 1 0.310 None 1.000 2 2005 2018
Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 4 0.300 None 1.000 2 2005 2007
CUI: C0002897
Disease: Anemia, Splenic
Anemia, Splenic
disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.300 None 1.000 1 2005 2005
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases Disease or Syndrome 24 52 0.330 None 1.000 1 2005 2015
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
group Cardiovascular Diseases Disease or Syndrome 48 455 0.510 None 1.000 1 1999 2007
Diabetes Mellitus, Non-Insulin-Dependent
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 221 1232 0.320 None 1.000 1 2005 2019
CUI: C0017658
Disease: Glomerulonephritis
Glomerulonephritis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 31 2 0.410 None 1.000 1 1999 2011
CUI: C0018939
Disease: Hematological Disease
Hematological Disease
group Hemic and Lymphatic Diseases Disease or Syndrome 8 0.300 None 1.000 1 2005 2005
CUI: C0020532
Disease: Hypersplenism
Hypersplenism
disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.400 None 1.000 1 2005 2005
CUI: C0024535
Disease: Malaria, Falciparum
Malaria, Falciparum
disease Infections Disease or Syndrome 4 0.300 None 1.000 1 2011 2011
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
disease Neoplasms; Immune System Diseases; Nervous System Diseases Disease or Syndrome 6 66 0.300 None 1.000 1 2003 2003
CUI: C0027697
Disease: Nephritis
Nephritis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 9 1 0.300 None 1.000 1 2015 2015
Pregnancy Complications, Cardiovascular
disease Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases Disease or Syndrome 4 0.300 None 1.000 1 2000 2000
CUI: C0039338
Disease: Taste Disorders
Taste Disorders
group Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 2 0.300 None 1.000 1 2012 2012
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
Uveomeningoencephalitic Syndrome
disease Eye Diseases; Immune System Diseases; Nervous System Diseases Disease or Syndrome 4 4 0.310 None 1.000 1 2015 2015
CUI: C0162557
Disease: Liver Failure, Acute
Liver Failure, Acute
disease Digestive System Diseases Disease or Syndrome 24 8 0.350 None 1.000 1 1995 2019
CUI: C0234297
Disease: Taste Disorder, Primary
Taste Disorder, Primary
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 2 0.300 None 1.000 1 2012 2012
CUI: C0234298
Disease: Taste Disorder, Primary, Sweet
Taste Disorder, Primary, Sweet
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 2 0.300 None 1.000 1 2012 2012
CUI: C0234299
Disease: Taste Disorder, Primary, Salt
Taste Disorder, Primary, Salt
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 2 0.300 None 1.000 1 2012 2012
CUI: C0234300
Disease: Taste Disorder, Primary, Bitter
Taste Disorder, Primary, Bitter
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 2 0.300 None 1.000 1 2012 2012