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: C0233514
Disease: Abnormal behavior
Abnormal behavior
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 910 121 0.010 None 1.000 1 2014 2014
CUI: C0000833
Disease: Abscess
Abscess
phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 96 1 0.040 None 1.000 4 2012 2017
CUI: C1854882
Disease: Absent speech
Absent speech
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 232 72 0.100 None 0
CUI: C4552483
Disease: ABSSSI
ABSSSI
disease Disease or Syndrome 2 0.040 None 1.000 4 2018 2020
CUI: C0702166
Disease: Acne
Acne
disease Skin and Connective Tissue Diseases Disease or Syndrome 167 11 0.010 None 1.000 1 2020 2020
CUI: C3554617
Disease: Adducted thumb
Adducted thumb
phenotype Musculoskeletal Diseases Finding 74 5 0.100 None 0
CUI: C0338106
Disease: Adenocarcinoma of colon
Adenocarcinoma of colon
disease Digestive System Diseases; Neoplasms Neoplastic Process 406 10 0.010 None 1.000 1 2017 2017
CUI: C0041228
Disease: African Trypanosomiasis
African Trypanosomiasis
disease Infections Disease or Syndrome 55 2 0.010 None 1.000 1 2019 2019
CUI: C4085595
Disease: AL-RAQAD SYNDROME
AL-RAQAD SYNDROME
disease Disease or Syndrome 17 8 0.010 None 1.000 1 2019 2019
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
disease Nervous System Diseases; Mental Disorders Disease or Syndrome 3397 1843 0.030 None 1.000 3 2015 2018
CUI: C0162635
Disease: Angelman Syndrome
Angelman Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 94 135 0.050 None 1.000 5 2008 2014
Aplasia/Hypoplasia of the cerebellum
phenotype Finding 116 5 0.100 None 0
Aplasia/Hypoplasia of the corpus callosum
phenotype Finding 108 8 0.100 None 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 198 33 0.100 None 0
Aspergillosis, Allergic Bronchopulmonary
disease Infections; Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 31 6 0.010 None 1.000 1 2009 2009
CUI: C0004134
Disease: Ataxia
Ataxia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 868 68 0.030 None 1.000 3 2011 2015
CUI: C0427190
Disease: Ataxia, Truncal
Ataxia, Truncal
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 68 13 0.100 None 0
CUI: C0041671
Disease: Attention Deficit Disorder
Attention Deficit Disorder
disease Mental Disorders Mental or Behavioral Dysfunction 123 7 0.010 None 1.000 1 2018 2018
Attention deficit hyperactivity disorder
disease Mental Disorders Mental or Behavioral Dysfunction 842 420 0.020 None 1.000 2 2016 2018
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
disease Mental Disorders Mental or Behavioral Dysfunction 1112 395 0.110 None 1.000 1 1 2014 2014
CUI: C0004610
Disease: Bacteremia
Bacteremia
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 233 7 0.100 None 0.926 27 2008 2020
Bacteremia due to Methicillin resistant Staphylococcus aureus
disease Disease or Syndrome 7 0.010 None 1.000 1 2013 2013
Bacteremia due to Staphylococcus aureus
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 17 1 0.080 None 0.875 8 2017 2019
CUI: C0014121
Disease: Bacterial Endocarditis
Bacterial Endocarditis
disease Infections; Cardiovascular Diseases Disease or Syndrome 68 9 0.070 None 0.857 7 2011 2017
CUI: C0004623
Disease: Bacterial Infections
Bacterial Infections
group Infections Disease or Syndrome 616 17 0.020 None 1.000 2 2017 2019