SUMF2, sulfatase modifying factor 2, 25870

N. diseases: 59; N. variants: 4
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: C1411966
Disease: Clostridium; difficile (disorder)
Clostridium; difficile (disorder) 		disease Disease or Syndrome 106 0.020 None 0.500 2 2005 2011
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		group Laboratory Procedure 53 92 0.100 None 1.000 1 1 2019 2019
CUI: C0428210
Disease: Methionine measurement
Methionine measurement 		phenotype Laboratory Procedure 3 4 0.100 None 1.000 1 1 2019 2019
CUI: C0523888
Disease: Serine measurement
Serine measurement 		phenotype Laboratory Procedure 9 18 0.100 None 1.000 1 1 2019 2019
CUI: C0523920
Disease: Threonine measurement
Threonine measurement 		phenotype Laboratory Procedure 4 5 0.100 None 1.000 1 1 2019 2019
CUI: C0742006
Disease: Catheter infection
Catheter infection 		disease Disease or Syndrome 3 0.010 None 1.000 1 2008 2008
CUI: C1318881
Disease: Vancomycin intermediate staphylococcus aureus infection
Vancomycin intermediate staphylococcus aureus infection 		disease Disease or Syndrome 16 0.010 None < 0.001 1 2011 2011
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 852 704 0.050 None 1.000 5 1989 2013
CUI: C1843256
Disease: IRAK4 Deficiency
IRAK4 Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 5 9 0.010 None 1.000 1 2007 2007
CUI: C0238288
Disease: Muscular Dystrophy, Facioscapulohumeral
Muscular Dystrophy, Facioscapulohumeral 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 143 3 0.010 None 1.000 1 1999 1999
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 384 698 0.010 None 1.000 1 1990 1990
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 130 1012 0.010 None 1.000 1 2006 2006
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		group Digestive System Diseases Disease or Syndrome 1577 605 0.010 None 1.000 1 2011 2011
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		disease Digestive System Diseases Disease or Syndrome 429 52 0.010 None 1.000 1 2012 2012
CUI: C0013371
Disease: Shigella Infections
Shigella Infections 		group Digestive System Diseases; Infections Disease or Syndrome 121 0.040 None 1.000 4 2007 2015
CUI: C0023885
Disease: Liver Abscess
Liver Abscess 		disease Digestive System Diseases; Infections Disease or Syndrome 22 1 0.010 None 1.000 1 2013 2013
CUI: C0275982
Disease: Enteric campylobacteriosis
Enteric campylobacteriosis 		disease Digestive System Diseases; Infections Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C0302358
Disease: Disease caused by Shigella dysenteriae
Disease caused by Shigella dysenteriae 		disease Digestive System Diseases; Infections Disease or Syndrome 15 0.010 None 1.000 1 2011 2011
CUI: C0302360
Disease: Disease caused by Shigella boydii
Disease caused by Shigella boydii 		disease Digestive System Diseases; Infections Disease or Syndrome 5 0.010 None 1.000 1 2008 2008
CUI: C0302361
Disease: Disease caused by Shigella sonnei
Disease caused by Shigella sonnei 		disease Digestive System Diseases; Infections Disease or Syndrome 11 0.010 None 1.000 1 2015 2015
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		disease Digestive System Diseases; Neoplasms Neoplastic Process 5473 1962 0.010 None 1.000 1 2019 2019
CUI: C0553694
Disease: Oropharyngeal disorders
Oropharyngeal disorders 		group Digestive System Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 163 3 0.010 None 1.000 1 2018 2018
CUI: C0022568
Disease: Keratitis
Keratitis 		disease Eye Diseases Disease or Syndrome 156 10 0.010 None 1.000 1 2013 2013
CUI: C0042029
Disease: Urinary tract infection
Urinary tract infection 		group Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 219 14 0.020 None 0.500 2 2010 2016
CUI: C0262655
Disease: Recurrent urinary tract infection
Recurrent urinary tract infection 		disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 237 21 0.010 None < 0.001 1 2016 2016