TST, thiosulfate sulfurtransferase, 7263

N. diseases: 91; N. variants: 10
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.
Butterfly-shaped pigmentary macular dystrophy
disease Disease or Syndrome 7 0.010 None 1.000 1 1996 1996
CUI: C0730366
Disease: Rod dystrophy
Rod dystrophy
disease Disease or Syndrome 2 2 0.010 None 1.000 1 1996 1996
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy
disease Eye Diseases Disease or Syndrome 48 31 0.010 None 1.000 1 1997 1997
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 6243 355 0.010 None 1.000 1 2018 2018
CUI: C0456909
Disease: Blindness
Blindness
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 393 34 0.010 None 1.000 1 2000 2000
CUI: C0456065
Disease: Infant, Extremely Low Birth Weight
Infant, Extremely Low Birth Weight
phenotype Disease or Syndrome 15 1 0.010 None 1.000 1 2019 2019
CUI: C0339513
Disease: Dominant drusen
Dominant drusen
disease Congenital Abnormality 4 2 0.010 None 1.000 1 2002 2002
CUI: C0272170
Disease: Shwachman syndrome
Shwachman syndrome
disease Disease or Syndrome 49 13 0.010 None 1.000 1 2018 2018
CUI: C0267468
Disease: Intussusception of rectum
Intussusception of rectum
phenotype Digestive System Diseases Acquired Abnormality 1 0.010 None 1.000 1 2018 2018
CUI: C0240066
Disease: Iron deficiency
Iron deficiency
disease Nutritional and Metabolic Diseases Disease or Syndrome 179 13 0.010 None 1.000 1 2018 2018
CUI: C0236734
Disease: Caffeine related disorders
Caffeine related disorders
group Mental or Behavioral Dysfunction 360 56 0.010 None 1.000 1 2017 2017
CUI: C0162429
Disease: Malnutrition
Malnutrition
disease Nutritional and Metabolic Diseases Disease or Syndrome 417 29 0.010 None 1.000 1 2014 2014
CUI: C0158940
Disease: Transitory tachypnea of newborn
Transitory tachypnea of newborn
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Disease or Syndrome 5 0.010 None 1.000 1 2005 2005
CUI: C0149771
Disease: Rectocele
Rectocele
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Acquired Abnormality 1 0.010 None 1.000 1 2018 2018
Autosomal Recessive Polycystic Kidney Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 69 317 0.010 None 1.000 1 1998 1998
CUI: C0852283
Disease: Respiratory Distress Syndrome
Respiratory Distress Syndrome
disease Disease or Syndrome 58 9 0.010 None 1.000 1 2019 2019
CUI: C0917801
Disease: Sleeplessness
Sleeplessness
phenotype Nervous System Diseases; Mental Disorders Sign or Symptom 174 30 0.010 None 1.000 1 2017 2017
Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus
disease Disease or Syndrome 3 0.010 None 1.000 1 2007 2007
CUI: C4288779
Disease: Major Congenital Anomaly
Major Congenital Anomaly
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 2 0.010 None 1.000 1 2019 2019
Pauci-immune Glomerulonephritis associated with Granulomatosis with Polyangiitis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 71 15 0.010 None 1.000 1 2005 2005
CUI: C3831078
Disease: Clinical Chorioamnionitis
Clinical Chorioamnionitis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 8 0.010 None 1.000 1 2019 2019
CUI: C3711368
Disease: Surfactant Dysfunction
Surfactant Dysfunction
disease Respiratory Tract Diseases Disease or Syndrome 10 0.010 None 1.000 1 2018 2018
CUI: C2830004
Disease: Somnolence
Somnolence
phenotype Pathological Conditions, Signs and Symptoms Mental or Behavioral Dysfunction 87 8 0.010 None 1.000 1 2017 2017
Steroid Sulfatase Deficiency Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 181 5 0.010 None 1.000 1 2017 2017
CUI: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder)
disease Disease or Syndrome 23 317 0.010 None 1.000 1 2007 2007