FAS, Fas cell surface death receptor, 355

N. diseases: 754; N. variants: 47
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: C0002897
Disease: Anemia, Splenic
Anemia, Splenic 		disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.300 None 1.000 1 2005 2005
CUI: C0856836
Disease: Systemic juvenile chronic arthritis
Systemic juvenile chronic arthritis 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 1 0.010 None 1.000 1 1999 1999
CUI: C0948109
Disease: Idiopathic neutropenia
Idiopathic neutropenia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.010 None 1.000 1 2008 2008
CUI: C1868990
Disease: Acute HIV syndrome
Acute HIV syndrome 		disease Disease or Syndrome 1 0.010 None 1.000 1 2000 2000
CUI: C4016044
Disease: SQUAMOUS CELL CARCINOMA, BURN SCAR-RELATED, SOMATIC
SQUAMOUS CELL CARCINOMA, BURN SCAR-RELATED, SOMATIC 		phenotype Finding 1 3 0.100 None 0 3
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
CUI: C0234302
Disease: Taste Disorder, Anterior Tongue
Taste Disorder, Anterior Tongue 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 2 0.300 None 1.000 1 2012 2012
CUI: C0234303
Disease: Taste Disorder, Secondary
Taste Disorder, Secondary 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 2 0.300 None 1.000 1 2012 2012
CUI: C0234304
Disease: Taste Disorder, Secondary, Sweet
Taste Disorder, Secondary, Sweet 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 2 0.300 None 1.000 1 2012 2012
CUI: C0234305
Disease: Taste Disorder, Secondary, Salt
Taste Disorder, Secondary, Salt 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 2 0.300 None 1.000 1 2012 2012
CUI: C0234306
Disease: Taste Disorder, Secondary, Bitter
Taste Disorder, Secondary, Bitter 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 2 0.300 None 1.000 1 2012 2012
CUI: C0234319
Disease: Taste Disorder, Posterior Tongue
Taste Disorder, Posterior Tongue 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 2 0.300 None 1.000 1 2012 2012
CUI: C0240327
Disease: Taste, Metallic
Taste, Metallic 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 2 0.300 None 1.000 1 2012 2012
CUI: C1112306
Disease: Adenoviral hepatitis
Adenoviral hepatitis 		disease Disease or Syndrome 2 0.010 None 1.000 1 2000 2000
CUI: C1866119
Disease: Autoimmune Lymphoproliferative Syndrome, Type IA
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 0.130 None 1.000 3 15 1999 2005
CUI: C4703376
Disease: Increased proportion of HLA DR+ T cells
Increased proportion of HLA DR+ T cells 		phenotype Finding 3 0.100 None 0
CUI: C2717884
Disease: Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
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: C0006112
Disease: Brain Diseases, Metabolic
Brain Diseases, Metabolic 		group Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 4 0.200 None 1.000 1 2005 2005
CUI: C0032963
Disease: Pregnancy Complications, Cardiovascular
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 4 0.300 None 1.000 1 2012 2012
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