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.
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 546 541 0.100 None 0.955 22 1991 2017
Autosomal dominant retinitis pigmentosa
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 85 65 0.100 None 1.000 22 1991 2009
CUI: C3714602
Disease: Staphylococcal toxic shock syndrome
Staphylococcal toxic shock syndrome
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 28 0.060 None 0.833 6 1991 2017
CUI: C0600327
Disease: Toxic Shock Syndrome
Toxic Shock Syndrome
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 61 0.060 None 0.833 6 1991 2017
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Disease or Syndrome 423 112 0.020 None 0.500 2 1992 2019
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
disease Eye Diseases Disease or Syndrome 685 663 0.100 None 1.000 14 1993 2014
CUI: C0339508
Disease: Hereditary macular dystrophy
Hereditary macular dystrophy
disease Congenital Abnormality 39 10 0.060 None 1.000 6 1993 2009
CUI: C0730292
Disease: Macular dystrophy
Macular dystrophy
disease Eye Diseases Disease or Syndrome 52 59 0.060 None 1.000 6 1993 2009
Retinitis punctata albescens (disorder)
disease Eye Diseases Disease or Syndrome 10 10 0.040 None 1.000 4 1 1993 1997
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
group Eye Diseases Disease or Syndrome 714 56 0.050 None 0.800 5 1994 2010
CUI: C0024437
Disease: Macular degeneration
Macular degeneration
disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 44 16 0.030 None 1.000 3 1994 2014
CUI: C1536451
Disease: Central areolar choroidal sclerosis
Central areolar choroidal sclerosis
disease Eye Diseases Disease or Syndrome 10 5 0.050 None 1.000 5 1995 2009
CUI: C4024762
Disease: Pattern dystrophy of the retina
Pattern dystrophy of the retina
disease Eye Diseases Disease or Syndrome 4 0.020 None 1.000 2 1995 2001
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 254 51 0.030 None 1.000 3 1996 1998
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 86 53 0.020 None 1.000 2 1996 1998
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 194 33 0.020 None 1.000 2 1996 1998
CUI: C0730366
Disease: Rod dystrophy
Rod dystrophy
disease Disease or Syndrome 2 2 0.010 None 1.000 1 1996 1996
CUI: C1842475
Disease: Retinitis Pigmentosa 7
Retinitis Pigmentosa 7
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 7 22 0.010 None 1.000 1 1996 1996
Butterfly-shaped pigmentary macular dystrophy
disease Disease or Syndrome 7 0.010 None 1.000 1 1996 1996
CUI: C1320640
Disease: Peripheral retinal degeneration
Peripheral retinal degeneration
disease Eye Diseases Disease or Syndrome 4 1 0.010 None 1.000 1 1996 1996
Adult-Onset Vitelliform Macular Dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 8 16 0.040 None 1.000 4 1997 2008
CUI: C0730362
Disease: Disorder of macula of retina
Disorder of macula of retina
group Eye Diseases Disease or Syndrome 49 24 0.020 None 1.000 2 1997 2003
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy
disease Eye Diseases Disease or Syndrome 48 31 0.010 None 1.000 1 1997 1997
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
group Eye Diseases Disease or Syndrome 219 227 0.050 None 1.000 5 1998 2007
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