SLC6A8, solute carrier family 6 member 8, 6535

N. diseases: 274; N. variants: 27
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: C0432072
Disease: Dysmorphic features
Dysmorphic features
disease Congenital Abnormality 439 617 0.100 None 1.000 11 1 2000 2017
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.030 None 1.000 3 2017 2018
CUI: C1868938
Disease: End stage cardiac failure
End stage cardiac failure
disease Disease or Syndrome 76 2 0.020 None 1.000 2 2018 2018
Malignant neoplasm of stomach stage IV
disease Neoplastic Process 78 7 0.010 None 1.000 1 2015 2015
Non-small cell lung cancer stage IIIB
disease Neoplastic Process 11 0.010 None 1.000 1 2019 2019
Secondary malignant neoplasm of vertebral column
disease Neoplastic Process 15 0.010 None 1.000 1 2018 2018
CUI: C0851265
Disease: Learning problems
Learning problems
disease Mental or Behavioral Dysfunction 4 0.010 None 1.000 1 2002 2002
CUI: C1167791
Disease: Skin toxicity
Skin toxicity
disease Disease or Syndrome 62 24 0.010 None 1.000 1 2018 2018
CUI: C1854776
Disease: Infantile cardiomyopathy
Infantile cardiomyopathy
disease Disease or Syndrome 5 1 0.010 None 1.000 1 1996 1996
Stage II Nasopharyngeal Carcinoma AJCC v7
disease Neoplastic Process 3 0.010 None 1.000 1 2017 2017
Locally Recurrent Malignant Neoplasm
disease Neoplastic Process 68 1 0.010 None 1.000 1 2017 2017
CUI: C3160953
Disease: Left ventricular dyssynchrony
Left ventricular dyssynchrony
disease Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C3272309
Disease: Coronary Venous Dissection
Coronary Venous Dissection
disease Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C0239234
Disease: Low set ears
Low set ears
disease Congenital Abnormality 489 64 0.100 None 0 1
CUI: C0240379
Disease: Open mouth (finding)
Open mouth (finding)
phenotype Finding 96 11 0.100 None 0
CUI: C0241240
Disease: Tall stature
Tall stature
phenotype Finding 79 14 0.100 None 0
CUI: C0332615
Disease: Myopathic facies
Myopathic facies
phenotype Finding 44 15 0.100 None 0
CUI: C0349588
Disease: Short stature
Short stature
phenotype Finding 1127 292 0.100 None 0
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies
phenotype Finding 271 106 0.100 None 0 1
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
disease Mental or Behavioral Dysfunction 1825 553 0.100 None 0
CUI: C1836047
Disease: Long face
Long face
phenotype Finding 182 12 0.100 None 0
CUI: C1837463
Disease: Narrow face
Narrow face
phenotype Finding 87 6 0.100 None 0
CUI: C1843367
Disease: Poor school performance
Poor school performance
phenotype Finding 211 411 0.100 None 0 1
CUI: C1845864
Disease: Poor hand-eye coordination
Poor hand-eye coordination
phenotype Finding 2 0.100 None 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive
phenotype Finding 172 1 0.100 None 0