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: C1846130
Disease: Mental retardation X-linked, South African type
Mental retardation X-linked, South African type 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 1 0.500 None 1.000 4 2008 2018
CUI: C0021355
Disease: Infective otitis externa
Infective otitis externa 		disease Pathological Conditions, Signs and Symptoms; Infections; Skin and Connective Tissue Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 1 0.010 None 1.000 1 2013 2013
CUI: C0157680
Disease: Carbuncle/furuncle
Carbuncle/furuncle 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C0238454
Disease: Cavernous Sinus Thrombosis
Cavernous Sinus Thrombosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2008 2008
CUI: C0259860
Disease: psychiatric emergencies
psychiatric emergencies 		disease Mental or Behavioral Dysfunction 1 0.010 None 1.000 1 2017 2017
CUI: C0578437
Disease: Ischemic foot
Ischemic foot 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 1 0.010 None 1.000 1 2009 2009
CUI: C0854328
Disease: Infection due to anaerobic bacteria
Infection due to anaerobic bacteria 		group Infections Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C2349529
Disease: Pneumonia due to methicillin susceptible Staphylococcus aureus
Pneumonia due to methicillin susceptible Staphylococcus aureus 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 1 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: C4552483
Disease: ABSSSI
ABSSSI 		disease Disease or Syndrome 2 0.040 None 1.000 4 2018 2020
CUI: C0343525
Disease: Lemierre Syndrome
Lemierre Syndrome 		disease Infections; Stomatognathic Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2011 2011
CUI: C0452221
Disease: Osteomyelitis of vertebra
Osteomyelitis of vertebra 		disease Infections; Musculoskeletal Diseases Disease or Syndrome 2 0.010 None < 0.001 1 2019 2019
CUI: C0851881
Disease: Enterococcal infection
Enterococcal infection 		disease Infections Disease or Syndrome 2 0.010 None 1.000 1 2003 2003
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: C1846133
Disease: Loss of ability to walk in first decade
Loss of ability to walk in first decade 		phenotype Finding 2 0.100 None 0
CUI: C0264515
Disease: Pneumonia, Necrotizing
Pneumonia, Necrotizing 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 3 0.050 None 1.000 5 2002 2020
CUI: C0029878
Disease: Otitis Externa
Otitis Externa 		disease Otorhinolaryngologic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2013 2013
CUI: C0238419
Disease: Fournier Gangrene
Fournier Gangrene 		disease Infections; Male Urogenital Diseases Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
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: C1855722
Disease: Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation
Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 4 30 0.010 None 1.000 1 2018 2018
CUI: C4021029
Disease: Conspicuously happy disposition
Conspicuously happy disposition 		phenotype Finding 4 0.100 None 0
CUI: C2678194
Disease: Mental Retardation, X-Linked, Syndromic, Christianson Type
Mental Retardation, X-Linked, Syndromic, Christianson Type 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 6 13 0.800 definitive 1.000 19 13 2008 2020
CUI: C0744130
Disease: Diabetic foot infection
Diabetic foot infection 		disease Disease or Syndrome 6 1 0.020 None 1.000 2 2014 2020
CUI: C0025064
Disease: Mediastinitis
Mediastinitis 		disease Respiratory Tract Diseases Disease or Syndrome 6 0.010 None 1.000 1 2009 2009
CUI: C0265736
Disease: Congenital anomaly of nose
Congenital anomaly of nose 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Congenital Abnormality 6 0.100 None 0