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.
CUI: C0017152
Disease: Gastritis
Gastritis 		disease Digestive System Diseases Disease or Syndrome 292 21 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
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia 		disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 83 21 0.100 None 0
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 615 42 0.100 None 0
CUI: C1858973
Disease: Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells
Elevated proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells 		phenotype Finding 5 0.100 None 0
CUI: C1858980
Disease: Platelet antibody positive
Platelet antibody positive 		phenotype Laboratory or Test Result 4 0.100 None 0
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Finding 523 30 0.100 None 0
CUI: C1858981
Disease: Antineutrophil antibody positivity
Antineutrophil antibody positivity 		phenotype Laboratory or Test Result 15 0.100 None 0
CUI: C0036572
Disease: Seizures
Seizures 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 2152 553 0.100 None 0
CUI: C0398650
Disease: Immune thrombocytopenic purpura
Immune thrombocytopenic purpura 		disease Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 338 35 0.100 None 0
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 92 14 0.100 None 0
CUI: C0423798
Disease: Increased tendency to bruise
Increased tendency to bruise 		phenotype Wounds and Injuries Finding 133 14 0.100 None 0
CUI: C0020532
Disease: Hypersplenism
Hypersplenism 		disease Hemic and Lymphatic Diseases Disease or Syndrome 22 0.100 None 0
CUI: C1866120
Disease: Autoimmune Lymphoproliferative Syndrome, Type IB
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: C0520736
Disease: Coombs positive hemolytic anemia
Coombs positive hemolytic anemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 6 0.100 None 0
CUI: C4021032
Disease: Abnormal vitamin B12 level
Abnormal vitamin B12 level 		phenotype Finding 5 0.100 None 0
CUI: C1839304
Disease: Decreased proportion of CD4-positive T cells
Decreased proportion of CD4-positive T cells 		phenotype Immune System Diseases; Hemic and Lymphatic Diseases Finding 19 0.100 None 0
CUI: C0235896
Disease: Pulmonary Infiltrate
Pulmonary Infiltrate 		phenotype Respiratory Tract Diseases Finding 43 0.100 None 0
CUI: C1858969
Disease: Decreased lymphocyte apoptosis
Decreased lymphocyte apoptosis 		phenotype Finding 5 0.100 None 0
CUI: C1858970
Disease: Chronic noninfectious lymphadenopathy
Chronic noninfectious lymphadenopathy 		phenotype Hemic and Lymphatic Diseases Finding 12 0.100 None 0
CUI: C0017658
Disease: Glomerulonephritis
Glomerulonephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 391 7 0.100 None 0
CUI: C1855710
Disease: Bone marrow hypocellularity
Bone marrow hypocellularity 		phenotype Finding 64 5 0.100 None 0
CUI: C0206160
Disease: Reticulocytosis
Reticulocytosis 		phenotype Pathological Conditions, Signs and Symptoms Finding 40 1 0.100 None 0
CUI: C4280772
Disease: Abnormal serum interleukin level
Abnormal serum interleukin level 		phenotype Finding 6 0.100 None 0
CUI: C0018681
Disease: Headache
Headache 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 338 75 0.100 None 0