SUMF2, sulfatase modifying factor 2, 25870

N. diseases: 59; N. variants: 4
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.050 Biomarker disease BEFREE Using a series of alternative genotyping approaches [PFGE, random amplification of polymorphic DNA (RAPD), variable number of tandem repeats (VNTR) and multilocus sequence typing (MLST)], the six CF clone D isolates and eight previously identified clone D isolates associated with infections leading to keratitis were compared. 23105019 2013
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.050 Biomarker disease BEFREE P. aeruginosa isolates (313 isolates from 142 sputum samples and 53 throat swabs) from 68 CF patients were examined using PFGE to explore the diversity of P. aeruginosa isolates among CF patients in a Dublin paediatric hospital. 21921114 2012
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.050 Biomarker disease BEFREE Linked rep-PCR profiles were observed for isolates recovered from a same family of cystic fibrosis (CF) patients, for the etiological agents of clustered cases of nosocomial infections, and for some isolates recovered from a same hospital room. rep-PCR and pulsed-field gel electrophoresis SpeI restricted genomic DNA (PFGE-SpeI) profiles were compared. 19449044 2009
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.050 Biomarker disease BEFREE This study investigated the PFGE genetic pattern and antimicrobial resistance profile of 42 A. xylosoxidans isolates obtained over 4 years from the respiratory tract of 22 CF patients. 19024606 2008
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.050 Biomarker disease BEFREE Using PFGE mapping and the three jump clones, we found it possible to orient D7S8 on the chromosome and, by linkage analysis, to further narrow the CF region by 100 kb. 2565081 1989