LTC4S, leukotriene C4 synthase, 4056

N. diseases: 50; N. variants: 3
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: C1319853
Disease: Asthma, Aspirin-Induced
Asthma, Aspirin-Induced
disease Respiratory Tract Diseases; Immune System Diseases; Chemically-Induced Disorders Disease or Syndrome 25 6 0.340 None 0.875 8 1997 2011
CUI: C0013182
Disease: Drug Allergy
Drug Allergy
group Immune System Diseases; Chemically-Induced Disorders Pathologic Function 37 0.300 None 1.000 1 2006 2006
CUI: C3279662
Disease: Leukotriene C4 Synthase Deficiency
Leukotriene C4 Synthase Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 1 0.300 None 0
CUI: C0017658
Disease: Glomerulonephritis
Glomerulonephritis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 391 7 0.200 None 1.000 1 1995 1995
CUI: C0162557
Disease: Liver Failure, Acute
Liver Failure, Acute
disease Digestive System Diseases Disease or Syndrome 282 21 0.200 None 1.000 1 2008 2008
CUI: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy
group Nervous System Diseases Disease or Syndrome 351 81 0.200 None 1.000 1 2010 2010
Non-Neoplastic Peripheral Nervous System Disorder
disease Nervous System Diseases Disease or Syndrome 3 0.200 None 1.000 1 2010 2010
CUI: C0004096
Disease: Asthma
Asthma
disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 2096 1536 0.100 None 1.000 28 2000 2019
CUI: C1858430
Disease: Death in infancy
Death in infancy
phenotype Finding 146 7 0.100 None 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 967 579 0.100 None 0
CUI: C0025958
Disease: Microcephaly
Microcephaly
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Congenital Abnormality 1064 27 0.100 None 0
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
disease Mental or Behavioral Dysfunction 1825 553 0.100 None 0
CUI: C1867873
Disease: Failure to thrive in infancy
Failure to thrive in infancy
phenotype Finding 97 12 0.100 None 0
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 1172 115 0.030 None 1.000 3 2000 2004
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1159 704 0.030 None 1.000 3 1 2009 2012
CUI: C0741250
Disease: aspirin sensitivity
aspirin sensitivity
phenotype Disease or Syndrome 10 0.020 None 1.000 2 2004 2007
CUI: C0085129
Disease: Bronchial Hyperreactivity
Bronchial Hyperreactivity
disease Respiratory Tract Diseases Disease or Syndrome 112 18 0.020 None 0.500 2 2003 2007
CUI: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma
disease Immune System Diseases Disease or Syndrome 133 46 0.020 None 1.000 2 1 2012 2012
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
group Cardiovascular Diseases Disease or Syndrome 1756 711 0.020 None 1.000 2 2009 2010
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1658 591 0.020 None 1.000 2 2007 2008
CUI: C0155877
Disease: Allergic asthma
Allergic asthma
disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 371 55 0.020 None 1.000 2 1 2012 2012
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 1800 680 0.020 None 1.000 2 2010 2016
CUI: C0004059
Disease: aspirin intolerance
aspirin intolerance
phenotype Sign or Symptom 23 4 0.020 None 1.000 2 2000 2004
CUI: C0035204
Disease: Respiration Disorders
Respiration Disorders
group Respiratory Tract Diseases Disease or Syndrome 208 6 0.010 None 1.000 1 2009 2009
CUI: C0007965
Disease: Chediak-Higashi Syndrome
Chediak-Higashi Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 41 14 0.010 None 1.000 1 2003 2003