SLC9A6, solute carrier family 9 member A6, 10479

N. diseases: 210; N. variants: 15
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: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		phenotype Neoplastic Process 6626 169 0.040 None 1.000 4 2011 2019
CUI: C4552483
Disease: ABSSSI
ABSSSI 		disease Disease or Syndrome 2 0.040 None 1.000 4 2018 2020
CUI: C1411966
Disease: Clostridium; difficile (disorder)
Clostridium; difficile (disorder) 		disease Disease or Syndrome 106 0.030 None 1.000 3 2013 2018
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease Mental or Behavioral Dysfunction 1825 553 0.120 None 1.000 2 2 2011 2014
CUI: C0744130
Disease: Diabetic foot infection
Diabetic foot infection 		disease Disease or Syndrome 6 1 0.020 None 1.000 2 2014 2020
CUI: C1318881
Disease: Vancomycin intermediate staphylococcus aureus infection
Vancomycin intermediate staphylococcus aureus infection 		disease Disease or Syndrome 16 0.020 None 1.000 2 2011 2018
CUI: C0259860
Disease: psychiatric emergencies
psychiatric emergencies 		disease Mental or Behavioral Dysfunction 1 0.010 None 1.000 1 2017 2017
CUI: C0548923
Disease: Burn infection
Burn infection 		disease Disease or Syndrome 7 0.010 None 1.000 1 2019 2019
CUI: C0683322
Disease: Mental impairment
Mental impairment 		disease Mental or Behavioral Dysfunction 67 14 0.010 None 1.000 1 2016 2016
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		disease Disease or Syndrome 321 67 0.110 None 1.000 1 2016 2016
CUI: C0851989
Disease: Bone and joint infections
Bone and joint infections 		group Disease or Syndrome 4 0.010 None 1.000 1 2013 2013
CUI: C1319193
Disease: Infection due to vancomycin resistant Staphylococcus aureus
Infection due to vancomycin resistant Staphylococcus aureus 		disease Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		disease Disease or Syndrome 1075 276 0.010 None 1.000 1 2010 2010
CUI: C3854222
Disease: Human immunodeficiency virus (HIV) II infection category B1
Human immunodeficiency virus (HIV) II infection category B1 		disease Disease or Syndrome 985 56 0.010 None 1.000 1 2012 2012
CUI: C4040349
Disease: Bacteremia due to Methicillin resistant Staphylococcus aureus
Bacteremia due to Methicillin resistant Staphylococcus aureus 		disease Disease or Syndrome 7 0.010 None 1.000 1 2013 2013
CUI: C4048329
Disease: Immunosuppression
Immunosuppression 		disease Disease or Syndrome 632 9 0.010 None 1.000 1 2018 2018
CUI: C4085595
Disease: AL-RAQAD SYNDROME
AL-RAQAD SYNDROME 		disease Disease or Syndrome 17 8 0.010 None 1.000 1 2019 2019
CUI: C4552480
Disease: Complicated skin and skin structure infection
Complicated skin and skin structure infection 		disease Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C4552482
Disease: CSSSI
CSSSI 		disease Disease or Syndrome 9 0.010 None 1.000 1 2017 2017
CUI: C0152421
Disease: Macrotia
Macrotia 		disease Congenital Abnormality 188 18 0.100 None 0
CUI: C0240379
Disease: Open mouth (finding)
Open mouth (finding) 		phenotype Finding 96 11 0.100 None 0
CUI: C0349588
Disease: Short stature
Short stature 		phenotype Finding 1127 292 0.100 None 0 1
CUI: C0424304
Disease: Inappropriate laughter
Inappropriate laughter 		phenotype Finding 7 2 0.100 None 0
CUI: C0426790
Disease: Narrow thorax
Narrow thorax 		phenotype Finding 112 18 0.100 None 0
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		phenotype Pathologic Function 306 12 0.100 None 0