FASLG, Fas ligand, 356

N. diseases: 398; N. variants: 6
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.
Autoimmune Lymphoproliferative Syndrome, Type IB
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 1 1 0.100 None 0 1
CUI: C1112306
Disease: Adenoviral hepatitis
Adenoviral hepatitis
disease Disease or Syndrome 2 0.010 None 1.000 1 2000 2000
Autoimmune Lymphoproliferative Syndrome, Type IA
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 3 15 0.010 None 1.000 1 2005 2005
Increased proportion of HLA DR+ T cells
phenotype Finding 3 0.100 None 0
CUI: C0241185
Disease: Smooth muscle antibodies positive
Smooth muscle antibodies positive
phenotype Laboratory or Test Result 4 0.100 None 0
CUI: C1843386
Disease: Reduced delayed hypersensitivity
Reduced delayed hypersensitivity
phenotype Finding 4 0.100 None 0
CUI: C1858980
Disease: Platelet antibody positive
Platelet antibody positive
phenotype Laboratory or Test Result 4 0.100 None 0
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 0
CUI: C0153373
Disease: Malignant neoplasm of cheek mucosa
Malignant neoplasm of cheek mucosa
disease Neoplasms; Stomatognathic Diseases Neoplastic Process 5 1 0.010 None 1.000 1 2015 2015
CUI: C1858969
Disease: Decreased lymphocyte apoptosis
Decreased lymphocyte apoptosis
phenotype Finding 5 0.100 None 0
CUI: C1858972
Disease: Increased B cell count
Increased B cell count
phenotype Hemic and Lymphatic Diseases Finding 5 0.100 None 0
Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells
phenotype Finding 5 0.100 None 0
CUI: C4021032
Disease: Abnormal vitamin B12 level
Abnormal vitamin B12 level
phenotype Finding 5 0.100 None 0
CUI: C4531156
Disease: Abnormal proportion of CD4 T cells
Abnormal proportion of CD4 T cells
phenotype Finding 5 0.100 None 0
CUI: C0866588
Disease: lupus erythematodes
lupus erythematodes
disease Disease or Syndrome 6 0.010 None 1.000 1 2001 2001
CUI: C0520736
Disease: Coombs positive hemolytic anemia
Coombs positive hemolytic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 6 0.100 None 0
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 6 14 0.100 None 0 1
Specific anti-polysaccharide antibody deficiency
phenotype Finding 6 0.100 None 0
CUI: C4280772
Disease: Abnormal serum interleukin level
Abnormal serum interleukin level
phenotype Finding 6 0.100 None 0
CUI: C4531155
Disease: Abnormal proportion of CD8 T cells
Abnormal proportion of CD8 T cells
phenotype Finding 6 0.100 None 0
Rheumatoid factor positive (finding)
phenotype Laboratory or Test Result 7 0.100 None 0
CUI: C1399819
Disease: Humoral immunodeficiency
Humoral immunodeficiency
disease Immune System Diseases Disease or Syndrome 9 4 0.010 None 1.000 1 2000 2000
CUI: C0600178
Disease: External Carotid Artery Diseases
External Carotid Artery Diseases
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 1.000 1 2004 2004
CUI: C0750986
Disease: Internal Carotid Artery Diseases
Internal Carotid Artery Diseases
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 1.000 1 2004 2004
CUI: C0750987
Disease: Arterial Diseases, Common Carotid
Arterial Diseases, Common Carotid
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 1.000 1 2004 2004